Trial Matcher - Create Job
Create Trial Matcher job
Creates a Trial Matcher job with the given request body.
POST {endpoint}/health-insights/trial-matcher/jobs?api-version=2023-09-01-previewURI Parameters
| Name | In | Required | Type | Description |
|---|---|---|---|---|
|
endpoint
|
path | True |
string uri |
Supported Cognitive Services endpoints (protocol and hostname, for example: https://westus2.api.cognitive.microsoft.com). |
|
api-version
|
query | True |
string |
The API version to use for this operation. |
Request Header
| Name | Required | Type | Description |
|---|---|---|---|
| Ocp-Apim-Subscription-Key | True |
string |
|
| Repeatability-Request-ID |
string |
An opaque, globally-unique, client-generated string identifier for the request. |
|
| Repeatability-First-Sent |
string date-time |
Specifies the date and time at which the request was first created. |
Request Body
| Name | Required | Type | Description |
|---|---|---|---|
| patients | True |
The list of patients, including their clinical information and data. |
|
| configuration |
Configuration affecting the Trial Matcher model's inference. |
Responses
| Name | Type | Description |
|---|---|---|
| 202 Accepted |
The request has been accepted for processing, but processing has not yet completed. Headers
|
|
| Other Status Codes |
An unexpected error response. Headers x-ms-error-code: string |
Security
Ocp-Apim-Subscription-Key
Type:
apiKey
In:
header
Examples
Creates a Trial Matcher job with the given request body.
Sample request
POST {endpoint}/health-insights/trial-matcher/jobs?api-version=2023-09-01-preview
{
"patients": [
{
"id": "Patient ID Example 2",
"info": {
"sex": "female",
"birthDate": "1976-09-10",
"clinicalInfo": [
{
"resourceType": "Condition",
"code": {
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "C0041296",
"display": "Tuberculosis"
}
]
}
},
{
"code": {
"coding": [
{
"code": "C0006826",
"display": "MalignantNeoplasms",
"system": "http://www.nlm.nih.gov/research/umls"
}
]
},
"resourceType": "Observation",
"status": "unknown",
"valueBoolean": true
},
{
"code": {
"coding": [
{
"code": "C0018802",
"display": "MalignantNeoplasms",
"system": "http://www.nlm.nih.gov/research/umls"
}
]
},
"resourceType": "Observation",
"status": "unknown",
"valueBoolean": true
}
]
}
}
],
"configuration": {
"verbose": true,
"includeEvidence": true,
"clinicalTrials": {
"customTrials": [
{
"resourceType": "ResearchStudy",
"contained": [
{
"resourceType": "PlanDefinition",
"id": "1b5bc5d5-9413-43f7-9da6-70db2606b7cd",
"name": "Rilpivirine",
"title": "Rilpivirine",
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/plan-definition-type",
"code": "workflow-definition",
"display": "Workflow Definition"
}
]
},
"status": "active",
"action": [
{
"title": "Rilpivirine",
"description": "Patients will receive rilpivirine tablet 25 milligram or adjusted dose orally once daily for 240 weeks.",
"code": [
{
"text": "Drug"
}
]
}
]
},
{
"resourceType": "PlanDefinition",
"id": "30f45f8a-a0f5-4eed-a5e1-4819137c10b2",
"name": "Zidovudine",
"title": "Zidovudine",
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/plan-definition-type",
"code": "workflow-definition",
"display": "Workflow Definition"
}
]
},
"status": "active",
"action": [
{
"title": "Zidovudine",
"description": "Type=exact, form= appropriate pediatric formulation, unit=mg, route=oral. The patients will receive this selected NRTI once daily for 240 weeks.",
"code": [
{
"text": "Drug"
}
]
}
]
},
{
"resourceType": "PlanDefinition",
"id": "8958e19c-17db-4152-874d-cf68c3918769",
"name": "Abacavir",
"title": "Abacavir",
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/plan-definition-type",
"code": "workflow-definition",
"display": "Workflow Definition"
}
]
},
"status": "active",
"action": [
{
"title": "Abacavir",
"description": "Type=exact, form=appropriate pediatric formulation, unit=mg, route=oral. The patients will receive this selected NRTI once daily for 240 weeks.",
"code": [
{
"text": "Drug"
}
]
}
]
},
{
"resourceType": "PlanDefinition",
"id": "bef1c7b6-1e1a-4fb4-8bcd-b9d965dd09e6",
"name": "Tenofovir disoproxil fumarate",
"title": "Tenofovir disoproxil fumarate",
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/plan-definition-type",
"code": "workflow-definition",
"display": "Workflow Definition"
}
]
},
"status": "active",
"action": [
{
"title": "Tenofovir disoproxil fumarate",
"description": "Type=exact, form=appropriate pediatric formulation, unit=mg, route=oral. The patients will receive this selected NRTI once daily for 240 weeks.",
"code": [
{
"text": "Drug"
}
]
}
]
},
{
"resourceType": "PlanDefinition",
"id": "ec554338-0167-4034-98dd-ee1cd5860430",
"name": "Lamivudine",
"title": "Lamivudine",
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/plan-definition-type",
"code": "workflow-definition",
"display": "Workflow Definition"
}
]
},
"status": "active",
"action": [
{
"title": "Lamivudine",
"description": "Type=exact, form=appropriate pediatric formulation, unit=mg, route=oral. The patients will receive this selected NRTI once daily for 240 weeks.",
"code": [
{
"text": "Drug"
}
]
}
]
},
{
"resourceType": "PlanDefinition",
"id": "8ddc695e-efab-441e-bd49-c1decfdb80bf",
"name": "Emtricitabine",
"title": "Emtricitabine",
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/plan-definition-type",
"code": "workflow-definition",
"display": "Workflow Definition"
}
]
},
"status": "active",
"action": [
{
"title": "Emtricitabine",
"description": "Type=exact, form=appropriate pediatric formulation, unit=mg, route=oral. The patients will receive this selected NRTI once daily for 240 weeks.",
"code": [
{
"text": "Drug"
}
]
}
]
},
{
"resourceType": "Group",
"id": "73e459c6-9b92-479d-b122-0712d18a9131",
"extension": [
{
"id": "GroupQuantifier",
"valueCoding": {
"system": "http://hl7.org/fhir/action-selection-behavior",
"code": "all",
"display": "All"
}
}
],
"type": "person",
"actual": false,
"characteristic": [
{
"code": {
"extension": [
{
"id": "CharacteristicCodeType",
"valueString": "TreatmentName"
}
],
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "C0723712",
"display": "therapeutic"
},
{
"system": "http://www.nlm.nih.gov/research/umls/rxnorm",
"code": "220281",
"display": "therapeutic"
},
{
"system": "http://www.nlm.nih.gov/research/umls/chv",
"code": "0000046327",
"display": "therapeutic"
},
{
"system": "http://www.nlm.nih.gov/research/umls/mmsl",
"code": "7381",
"display": "therapeutic"
}
],
"text": "therapeutic"
},
"valueCodeableConcept": {
"coding": [
{
"system": "http://loinc.org",
"code": "47519-4",
"display": "History of Procedures"
}
],
"text": "History of Procedures"
},
"exclude": false
},
{
"code": {
"extension": [
{
"id": "CharacteristicCodeType",
"valueString": "TreatmentName"
}
],
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "C0086413",
"display": "HIV vaccine"
},
{
"system": "http://ncimeta.nci.nih.gov",
"code": "C1325",
"display": "HIV vaccine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/medcin",
"code": "347399",
"display": "HIV vaccine"
},
{
"system": "http://hl7.org/fhir/sid/cvx",
"code": "61",
"display": "HIV vaccine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/hl7v2.5",
"code": "61",
"display": "HIV vaccine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/hl7v3.0",
"code": "61",
"display": "HIV vaccine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/msh",
"code": "D016915",
"display": "HIV vaccine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/chv",
"code": "0000015914",
"display": "HIV vaccine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/csp",
"code": "3059-5000",
"display": "HIV vaccine"
},
{
"system": "http://loinc.org",
"code": "LP183501-8",
"display": "HIV vaccine"
}
],
"text": "HIV vaccine"
},
"valueCodeableConcept": {
"coding": [
{
"system": "http://loinc.org",
"code": "47519-4",
"display": "History of Procedures"
}
],
"text": "History of Procedures"
},
"exclude": false
}
]
},
{
"resourceType": "Group",
"id": "127161fc-b30f-4efc-ae14-2d064dc6084b",
"extension": [
{
"id": "GroupQuantifier",
"valueCoding": {
"system": "http://hl7.org/fhir/action-selection-behavior",
"code": "all",
"display": "All"
}
}
],
"type": "person",
"actual": false,
"characteristic": [
{
"code": {
"text": "LogicalGroup"
},
"valueReference": {
"reference": "#73e459c6-9b92-479d-b122-0712d18a9131",
"type": "Group"
},
"exclude": true
},
{
"code": {
"extension": [
{
"id": "CharacteristicCodeType",
"valueString": "MedicationClass"
}
],
"text": "HIV drug",
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "somecode",
"display": "somecode"
}
]
},
"valueCodeableConcept": {
"coding": [
{
"system": "http://loinc.org",
"code": "10160-0",
"display": "History of medication use"
}
],
"text": "History of medication use"
},
"exclude": false
}
]
},
{
"resourceType": "Group",
"id": "c26ff014-3da3-419b-9338-6e4b4d49031e",
"extension": [
{
"id": "GroupQuantifier",
"valueCoding": {
"system": "http://hl7.org/fhir/action-selection-behavior",
"code": "one-or-more",
"display": "One Or More"
}
}
],
"type": "person",
"actual": false,
"characteristic": [
{
"code": {
"extension": [
{
"id": "CharacteristicCodeType",
"valueString": "MedicationName"
}
],
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "C0132326",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/msh",
"code": "D019829",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/drugbank",
"code": "DB00238",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/pdq",
"code": "CDR0000712787",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_fda",
"code": "99DK7FVK1H",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/mthspl",
"code": "99DK7FVK1H",
"display": "nevirapine"
},
{
"system": "http://hl7.org/fhir/ndfrt",
"code": "4020991",
"display": "nevirapine"
},
{
"system": "http://ncimeta.nci.nih.gov",
"code": "C29277",
"display": "nevirapine"
},
{
"system": "http://snomed.info/sctv",
"code": "108704001",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/medcin",
"code": "75157",
"display": "nevirapine"
},
{
"system": "http://www.whocc.no/atc",
"code": "J05AG01",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nddf",
"code": "006062",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/rcd",
"code": "eiK..",
"display": "nevirapine"
},
{
"system": "http://loinc.org",
"code": "LP21317-0",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/mmsl",
"code": "175112",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/lch_nw",
"code": "sh2010013984",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/chv",
"code": "0000016392",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/gs",
"code": "2030",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/csp",
"code": "4007-0088",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/rxnorm",
"code": "53654",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/usp",
"code": "m56485",
"display": "nevirapine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/uspmg",
"code": "MTHU000656",
"display": "nevirapine"
}
],
"text": "nevirapine"
},
"valueCodeableConcept": {
"coding": [
{
"system": "http://loinc.org",
"code": "10160-0",
"display": "History of medication use"
}
],
"text": "History of medication use"
},
"exclude": false
},
{
"code": {
"extension": [
{
"id": "CharacteristicCodeType",
"valueString": "MedicationName"
}
],
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "C0043474",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/pdq",
"code": "CDR0000040121",
"display": "zidovudine"
},
{
"system": "http://ncimeta.nci.nih.gov",
"code": "C947",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/msh",
"code": "D015215",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/csp",
"code": "2109-4800",
"display": "zidovudine"
},
{
"system": "http://snomed.info/sctv",
"code": "387151007",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/psy",
"code": "05223",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/medcin",
"code": "41905",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/drugbank",
"code": "DB00495",
"display": "zidovudine"
},
{
"system": "http://snomed.info/sct",
"code": "C-55B60",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/rcd",
"code": "ei5..",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/chv",
"code": "0000013273",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_nci-gloss",
"code": "CDR0000044478",
"display": "zidovudine"
},
{
"system": "http://hl7.org/fhir/ndfrt",
"code": "4019502",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/rxnorm",
"code": "11413",
"display": "zidovudine"
},
{
"system": "http://loinc.org",
"code": "LP16744-2",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_dtp",
"code": "NSC0602670",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/usp",
"code": "m89510",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/mthspl",
"code": "4B9XT59T7S",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/gs",
"code": "2650",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_ctrp",
"code": "C947",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_fda",
"code": "4B9XT59T7S",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/mmsl",
"code": "d00034",
"display": "zidovudine"
},
{
"system": "http://www.whocc.no/atc",
"code": "J05AF01",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/uspmg",
"code": "MTHU000671",
"display": "zidovudine"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nddf",
"code": "003019",
"display": "zidovudine"
}
],
"text": "zidovudine"
},
"valueCodeableConcept": {
"coding": [
{
"system": "http://loinc.org",
"code": "10160-0",
"display": "History of medication use"
}
],
"text": "History of medication use"
},
"exclude": false
}
]
},
{
"resourceType": "Group",
"id": "9ab418f5-9bf1-4bb7-a55f-0eed1244addb",
"extension": [
{
"id": "GroupQuantifier",
"valueCoding": {
"system": "http://hl7.org/fhir/action-selection-behavior",
"code": "all",
"display": "All"
}
}
],
"type": "person",
"actual": false,
"characteristic": [
{
"code": {
"text": "LogicalGroup"
},
"valueReference": {
"reference": "#c26ff014-3da3-419b-9338-6e4b4d49031e",
"type": "Group"
},
"exclude": false
},
{
"code": {
"extension": [
{
"id": "CharacteristicCodeType",
"valueString": "SymptomOrSign"
}
],
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "C0282474",
"display": "mother-to-child transmission"
},
{
"system": "http://www.nlm.nih.gov/research/umls/msh",
"code": "D018445",
"display": "mother-to-child transmission"
}
],
"text": "mother-to-child transmission"
},
"exclude": false
}
]
},
{
"resourceType": "Group",
"id": "c31f130b-c0e7-411a-a32b-57f07ea62559",
"extension": [
{
"id": "GroupQuantifier",
"valueCoding": {
"system": "http://hl7.org/fhir/action-selection-behavior",
"code": "all",
"display": "All"
}
}
],
"type": "person",
"actual": false,
"characteristic": [
{
"code": {
"text": "LogicalGroup"
},
"valueReference": {
"reference": "#127161fc-b30f-4efc-ae14-2d064dc6084b",
"type": "Group"
},
"exclude": false
},
{
"code": {
"text": "LogicalGroup"
},
"valueReference": {
"reference": "#9ab418f5-9bf1-4bb7-a55f-0eed1244addb",
"type": "Group"
},
"exclude": false
}
]
},
{
"resourceType": "Group",
"id": "1d943af4-3b3e-4363-9e82-bc0e59b8c3e1",
"extension": [
{
"id": "GroupQuantifier",
"valueCoding": {
"system": "http://hl7.org/fhir/action-selection-behavior",
"code": "one-or-more",
"display": "One Or More"
}
}
],
"type": "person",
"actual": false,
"characteristic": [
{
"code": {
"extension": [
{
"id": "CharacteristicCodeType",
"valueString": "MedicationName"
}
],
"coding": [
{
"system": "http://www.nlm.nih.gov/research/umls",
"code": "C0132326",
"display": "NVP"
},
{
"system": "http://www.nlm.nih.gov/research/umls/msh",
"code": "D019829",
"display": "NVP"
},
{
"system": "http://www.nlm.nih.gov/research/umls/drugbank",
"code": "DB00238",
"display": "NVP"
},
{
"system": "http://www.nlm.nih.gov/research/umls/pdq",
"code": "CDR0000712787",
"display": "NVP"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_fda",
"code": "99DK7FVK1H",
"display": "NVP"
},
{
"system": "http://www.nlm.nih.gov/research/umls/mthspl",
"code": "99DK7FVK1H",
"display": "NVP"
},
{
"system": "http://hl7.org/fhir/ndfrt",
"code": "4020991",
"display": "NVP"
},
{
"system": "http://ncimeta.nci.nih.gov",
"code": "C29277",
"display": "NVP"
},
{
"system": "http://snomed.info/sctv",
"code": "108704001",
"display": "NVP"
},
{
"system": "http://www.nlm.nih.gov/research/umls/medcin",
"code": "75157",
"display": "NVP"
},
{
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{
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"code": "39922",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://hl7.org/fhir/sid/icd-10",
"code": "D84.9",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_nci-gloss",
"code": "CDR0000045724",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"code": "D84.9",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://hl7.org/fhir/sid/icd-10",
"code": "D84.9",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://snomed.info/sct",
"code": "D-4600",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/csp",
"code": "1560-5885",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/mdr",
"code": "10021460",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/chv",
"code": "0000006602",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://ncimeta.nci.nih.gov",
"code": "C3131",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/hpo",
"code": "HP:0002721",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/omim",
"code": "MTHU032911",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://snomed.info/sct",
"code": "234532001",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://hl7.org/fhir/sid/icpc-2",
"code": "B99011",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_fda",
"code": "2156",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/msh",
"code": "D007153",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nci_nichd",
"code": "C39725",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://hl7.org/fhir/sid/icd-9-cm",
"code": "279.3",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/rcd",
"code": "X20GZ",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://snomed.info/sct",
"code": "F-C0450",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/costar",
"code": "U000355",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://loinc.org",
"code": "MTHU054768",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/nanda-i",
"code": "02515",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/lch_nw",
"code": "sh85064574",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/ccpss",
"code": "1007151",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://hl7.org/fhir/sid/icpc-2",
"code": "MTHU037620",
"display": "Immunologic Deficiency Syndromes"
},
{
"system": "http://www.nlm.nih.gov/research/umls/aod",
"code": "0000004832",
"display": "Immunologic Deficiency Syndromes"
}
],
"text": "Immunologic Deficiency Syndromes"
},
{
"coding": [
{
"system": "http://hl7.org/fhir/administrative-gender",
"code": "Unknown",
"display": "Unknown"
}
],
"text": "Unknown"
},
{
"coding": [
{
"system": "http://decades-value-set.ctm.microsoft.org",
"code": "0",
"display": "Age keyword for indexing - 0"
}
],
"text": "Age keyword for indexing - 0"
},
{
"coding": [
{
"system": "http://decades-value-set.ctm.microsoft.org",
"code": "10",
"display": "Age keyword for indexing - 10"
}
],
"text": "Age keyword for indexing - 10"
}
],
"description": "This is a Phase II, open-label (all people involved know the identity of the assigned drug)\r\n and single arm study. The study will consist of a screening period of maximum 8 weeks, an\r\n initial treatment period of 48 weeks, a post week 48 treatment extension period of 4 years,\r\n and a 4 week follow-up period. A follow-up period will take place regardless of the presence\r\n of serious adverse events (SAEs) if patients withdraw early (ie, before Week 48) or if\r\n patients do not participate in the extension after Week 48; after Week 48, a 4-week follow-up\r\n visit is only required in case of ongoing (S)AEs at the final on treatment visit. The initial\r\n 48-week treatment period will be structured into 2 age Cohorts; Cohort 1 (Aged greater than\r\n or equal to [>=] 12 to less than [<] 18 years) and Cohort 2 (Children Aged >= 6 to < 12\r\n years) and each Cohort will have 2 parts. The first part of the trial (Part 1) is designed to\r\n evaluate the steady-state pharmacokinetic (PK) profile and the short-term safety and\r\n antiviral activity of rilpivirine 25 mg or adjusted dose once daily when administered in\r\n combination with 2 NRTIs. At Week 2/4, intensive PK will be done and an analysis together\r\n with short-term safety and antiviral activity will be reviewed by a data monitoring committee\r\n (DMC). For adolescents (Cohort 1) if the mean steady-state exposure in this first group of\r\n patients is comparable to that of the adult population (ie, is within 80-125 percentage of\r\n the mean exposure of the 25 mg once daily dose group in study, TMC278-C204), and the Week 2/4\r\n safety and antiviral activity results have been reviewed and deemed satisfactory by the DMC,\r\n the second part of the trial will start. The second part of the trial will evaluate long-term\r\n (48 weeks and 240 weeks) safety, efficacy, and pharmacokinetics of rilpivirine in combination\r\n with the background regimen of 2 NRTIs with a primary analysis time point at 24 weeks. For\r\n patients aged greater than or equal to (>=) 6 to less than (<) 12 years (Cohort 2), after\r\n being treated for at least 4 weeks and the Week 2 intensive PK and Week 4 safety and\r\n antiviral activity have been reviewed and results are satisfactory, recruitment in Part 1\r\n will resume and additional subjects will be enrolled to have at least 10 subjects in Part 1.\r\n Once an appropriate RPV dose has been selected, Part 1 of Cohort 2 will be considered\r\n complete and Part 2 will start. All patients from Part 1 will roll over in Part 2 and\r\n additional patients will be recruited in Part 2 to have at least 25 subjects (including those\r\n from Part 1) overall. In both cohorts of the trial, the ART will consist of rilpivirine 25 mg\r\n or adjusted dose once daily and an investigator-selected background regimen containing 2\r\n NRTIs. Patients safety will be monitored throughout the study and during the follow up\r\n visits.",
"enrollment": [
{
"reference": "#2a43edc4-0000-0000-0000-000000000000",
"type": "Group"
}
],
"period": {
"start": "2011-01",
"end": "2027-08"
},
"arm": [
{
"name": "Rilpivirine (TMC278)",
"type": {
"text": "Experimental"
},
"description": "The patients will receive rilpivirine with 2 nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) as a background regimen in Cohort 1 [Aged greater than or equal to (> =) 12 to less than (<) 18 years] and Cohort 2 (children aged > = 6 to < 12 years). The NRTIs includes zidovudine, abacavir, or tenofovir disoproxil fumarate in combination with lamivudine or emtricitabine."
}
]
}
],
"registryFilters": [
{
"studyTypes": [
"interventional",
"observational"
],
"recruitmentStatuses": [
"recruiting",
"enrollingByInvitation"
],
"phases": [
"phase2",
"phase3"
],
"purposes": [
"diagnostic",
"prevention",
"basicScience"
],
"sources": [
"clinicaltrials.gov"
],
"facilityLocations": [
{
"city": "Basel",
"countryOrRegion": "Switzerland"
},
{
"city": "Allschwil",
"countryOrRegion": "Switzerland"
}
]
},
{
"sponsors": [
"Janssen"
],
"sources": [
"clinicaltrials.gov"
],
"facilityAreas": [
{
"type": "Feature",
"geometry": {
"type": "Point",
"coordinates": [
7.588576,
47.559601
]
},
"properties": {
"subType": "Circle",
"radius": 80000
}
}
]
},
{
"ids": [
"NCT04006015",
"NCT04545788",
"NCT04773711"
],
"sources": [
"clinicaltrials.gov"
]
}
]
}
}
}
Sample response
Operation-Location: {endpoint}/health-insights/trial-matcher/jobs/{id}?api-version=2023-09-01-preview
Retry-After: 1{
"status": "notStarted",
"id": "a4d3d73e-2be3-4ca1-bd4f-66a5bdd19754"
}Definitions
| Name | Description |
|---|---|
|
Area |
|
|
Area |
|
| Arm |
Defined path through the study for a subject |
|
Azure. |
The error object. |
|
Azure. |
A response containing error details. |
|
Azure. |
An object containing more specific information about the error. As per Microsoft One API guidelines - https://github.com/Microsoft/api-guidelines/blob/vNext/Guidelines.md#7102-error-condition-responses. |
|
Clinical |
The type of the clinical document. |
|
Clinical |
Possible phases of a clinical trial. |
|
Clinical |
Possible purposes of a clinical trial. |
|
Clinical |
Possible recruitment status of a clinical trial. |
|
Clinical |
A filter defining a subset of clinical trials from a given clinical trial registry (e.g. clinicaltrials.gov). |
|
Clinical |
The clinical trials that the patient(s) should be matched to. The trial selection can be given as a list of custom clinical trials and/or a list of filters to known clinical trial registries. In case both are given, the resulting trial set is a union of the two sets. |
|
Clinical |
Possible sources of a clinical trial. |
|
Clinical |
Possible study types of a clinical trial. |
|
Contact |
phone | fax | email | pager | url | sms | other |
|
Contact |
home | work | temp | old | mobile - purpose of this contact point |
|
Document |
Document administrative metadata |
|
Document |
Document author |
|
Document |
The content of the patient document. |
|
Document |
The type of the content's source. In case the source type is 'inline', the content is given as a string (for instance, text). In case the source type is 'reference', the content is given as a URI. |
|
Document |
The type of the patient document, such as 'note' (text document) or 'fhirBundle' (FHIR JSON document). |
| Encounter |
visit/encounter information |
|
Encounter |
Known values codes that can be used to indicate the class of encounter (TODO://Based on FHIR value set--http://....). |
|
Fhir. |
A text note which also contains information about who made the statement and when Based on FHIR Annotation |
|
Fhir. |
Concept - reference to a terminology or just text Based on FHIR CodeableConcept |
|
Fhir. |
A Coding is a representation of a defined concept using a symbol from a defined "code system". Based on FHIR Coding |
|
Fhir. |
Contact details (See: https://www.hl7.org/fhir/R4/metadatatypes.html#ContactDetail) |
|
Fhir. |
Details for all kinds of technology mediated contact points for a person or organization, including telephone, email, etc. See https://www.hl7.org/fhir/R4/datatypes.html#ContactPoint |
|
Fhir. |
Base for all elements Based on FHIR Element |
|
Fhir. |
An identifier intended for computation Based on FHIR Identifier |
|
Fhir. |
Metadata about a resource Based on FHIR Meta |
|
Fhir. |
Any resource that is a DomainResource may include a human-readable narrative that contains a summary of the resource and may be used to represent the content of the resource to a human. Based on FHIR Narrative |
|
Fhir. |
A time period defined by a start and end date and optionally time Based on FHIR Period |
|
Fhir. |
A measured or measurable amount Based on FHIR Quantity |
|
Fhir. |
A set of ordered Quantities defined by a low and high limit Based on FHIR Range |
|
Fhir. |
A ratio of two Quantity values - a numerator and a denominator Based on FHIR Ratio |
|
Fhir. |
A reference from one resource to another Based on FHIR Reference |
|
Fhir. |
Detailed information about Research Study Based on FHIR ResearchStudy |
|
Fhir. |
Resource is the ancestor of DomainResource from which most resources are derived. Bundle, Parameters, and Binary extend Resource directly. Based on [FHIR Resource](https://www.hl7.org/fhir/r4/resource.html |
|
Fhir. |
A series of measurements taken by a device Based on FHIR SampledData |
|
Geographic |
A geographic area, expressed as a |
|
Geographic |
A location given as a combination of city, state and country/region. It could specify a city, a state or a country/region. In case a city is specified, either state +country/region or country/region (for countries/regions where there are no states) should be added. In case a state is specified (without a city), country/region should be added. |
|
Geo |
|
|
Geo |
|
|
Geo |
|
| Objective |
A goal for the study |
|
Ordered |
Procedure information |
|
Patient |
A clinical document related to a patient. Document here is in the wide sense - not just a text document (note). |
|
Patient |
Patient structured information, including demographics and known structured clinical information. |
|
Patient |
The patient's sex. |
|
Patient |
A patient record, including their clinical information and data. |
|
Research |
active | administratively-completed | approved | closed-to-accrual | closed-to-accrual-and-intervention | completed | disapproved | in-review | temporarily-closed-to-accrual | temporarily-closed-to-accrual-and-intervention | withdrawn |
|
Specialty |
Known values codes that can be used to indicate the type of the Specialty. |
|
Time |
A duration of time during which an event is happening |
|
Trial |
The body of the Trial Matcher request. |
|
Trial |
Configuration affecting the Trial Matcher model's inference. |
AreaGeometry
GeoJSON geometry, representing the area circle's center.
| Name | Type | Description |
|---|---|---|
| coordinates |
number[] |
Coordinates of the area circle's center, represented according to the |
| type |
|
AreaProperties
GeoJSON object properties.
| Name | Type | Description |
|---|---|---|
| radius |
number |
The radius of the area's circle, in meters. |
| subType |
|
Arm
Defined path through the study for a subject
| Name | Type | Description |
|---|---|---|
| description |
string |
Short explanation of study path |
| name |
string |
Label for study arm |
| type |
Categorization of study arm |
Azure.Core.Foundations.Error
The error object.
| Name | Type | Description |
|---|---|---|
| code |
string |
One of a server-defined set of error codes. |
| details |
An array of details about specific errors that led to this reported error. |
|
| innererror |
An object containing more specific information than the current object about the error. |
|
| message |
string |
A human-readable representation of the error. |
| target |
string |
The target of the error. |
Azure.Core.Foundations.ErrorResponse
A response containing error details.
| Name | Type | Description |
|---|---|---|
| error |
The error object. |
Azure.Core.Foundations.InnerError
An object containing more specific information about the error. As per Microsoft One API guidelines - https://github.com/Microsoft/api-guidelines/blob/vNext/Guidelines.md#7102-error-condition-responses.
| Name | Type | Description |
|---|---|---|
| code |
string |
One of a server-defined set of error codes. |
| innererror |
Inner error. |
ClinicalDocumentType
The type of the clinical document.
| Name | Type | Description |
|---|---|---|
| consultation |
string |
|
| dischargeSummary |
string |
|
| historyAndPhysical |
string |
|
| laboratory |
string |
|
| pathologyReport |
string |
|
| procedure |
string |
|
| progress |
string |
|
| radiologyReport |
string |
ClinicalTrialPhase
Possible phases of a clinical trial.
| Name | Type | Description |
|---|---|---|
| earlyPhase1 |
string |
|
| notApplicable |
string |
|
| phase1 |
string |
|
| phase2 |
string |
|
| phase3 |
string |
|
| phase4 |
string |
ClinicalTrialPurpose
Possible purposes of a clinical trial.
| Name | Type | Description |
|---|---|---|
| basicScience |
string |
|
| deviceFeasibility |
string |
|
| diagnostic |
string |
|
| healthServicesResearch |
string |
|
| notApplicable |
string |
|
| other |
string |
|
| prevention |
string |
|
| screening |
string |
|
| supportiveCare |
string |
|
| treatment |
string |
ClinicalTrialRecruitmentStatus
Possible recruitment status of a clinical trial.
| Name | Type | Description |
|---|---|---|
| enrollingByInvitation |
string |
|
| notYetRecruiting |
string |
|
| recruiting |
string |
|
| unknownStatus |
string |
ClinicalTrialRegistryFilter
A filter defining a subset of clinical trials from a given clinical trial registry (e.g. clinicaltrials.gov).
| Name | Type | Description |
|---|---|---|
| conditions |
string[] |
Trials with any of the given medical conditions will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the medical conditions. |
| facilityAreas |
Trials with any of the given facility area boundaries will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the trial facility area boundaries. |
|
| facilityLocations |
Trials with any of the given facility locations will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the trial facility locations. |
|
| facilityNames |
string[] |
Trials with any of the given facility names will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the trial facility names. |
| ids |
string[] |
Trials with any of the given identifiers will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the trial identifiers. |
| phases |
Trials with any of the given phases will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the phases. |
|
| purposes |
Trials with any of the given purposes will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the purposes. |
|
| recruitmentStatuses |
Trials with any of the given recruitment statuses will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the recruitment statuses. |
|
| sources |
Trials with any of the given sources will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the sources. |
|
| sponsors |
string[] |
Trials with any of the given sponsors will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the sponsors. |
| studyTypes |
Trials with any of the given study types will be included in the selection (provided that other limitations are satisfied). Leaving this list empty will not limit the study types. |
ClinicalTrials
The clinical trials that the patient(s) should be matched to. The trial selection can be given as a list of custom clinical trials and/or a list of filters to known clinical trial registries. In case both are given, the resulting trial set is a union of the two sets.
| Name | Type | Description |
|---|---|---|
| customTrials |
A list of clinical trials. |
|
| registryFilters |
A list of filters, each one creating a selection of trials from a given clinical trial registry. |
ClinicalTrialSource
Possible sources of a clinical trial.
| Name | Type | Description |
|---|---|---|
| clinicaltrials.gov |
string |
|
| custom |
string |
ClinicalTrialStudyType
Possible study types of a clinical trial.
| Name | Type | Description |
|---|---|---|
| expandedAccess |
string |
|
| interventional |
string |
|
| observational |
string |
|
| patientRegistries |
string |
ContactPointSystem
phone | fax | email | pager | url | sms | other
| Name | Type | Description |
|---|---|---|
|
string |
|
|
| fax |
string |
Fax |
| other |
string |
Other |
| pager |
string |
Pager |
| phone |
string |
Phone |
| sms |
string |
Sms |
| url |
string |
Url |
ContactPointUse
home | work | temp | old | mobile - purpose of this contact point
| Name | Type | Description |
|---|---|---|
| home |
string |
Home |
| mobile |
string |
Mobile |
| old |
string |
Old |
| temp |
string |
Temp |
| work |
string |
Work |
DocumentAdministrativeMetadata
Document administrative metadata
| Name | Type | Description |
|---|---|---|
| encounterId |
string |
Reference to the encounter associated with the document. |
| orderedProcedures |
List of procedure information associated with the document. |
DocumentAuthor
Document author
| Name | Type | Description |
|---|---|---|
| fullName |
string |
Text representation of the full name |
| id |
string |
author id |
DocumentContent
The content of the patient document.
| Name | Type | Description |
|---|---|---|
| sourceType |
The type of the content's source. In case the source type is 'inline', the content is given as a string (for instance, text). In case the source type is 'reference', the content is given as a URI. |
|
| value |
string |
The content of the document, given either inline (as a string) or as a reference (URI). |
DocumentContentSourceType
The type of the content's source. In case the source type is 'inline', the content is given as a string (for instance, text). In case the source type is 'reference', the content is given as a URI.
| Name | Type | Description |
|---|---|---|
| inline |
string |
The content is given as a string (for instance, text). |
| reference |
string |
The content is given as a URI. |
DocumentType
The type of the patient document, such as 'note' (text document) or 'fhirBundle' (FHIR JSON document).
| Name | Type | Description |
|---|---|---|
| dicom |
string |
|
| fhirBundle |
string |
|
| genomicSequencing |
string |
|
| note |
string |
Encounter
visit/encounter information
| Name | Type | Description |
|---|---|---|
| class |
The class of the encounter. |
|
| id |
string |
The id of the visit. |
| period |
Time period of the visit. In case of admission, use timePeriod.start to indicate the admission time and timePeriod.end to indicate the discharge time. |
EncounterClass
Known values codes that can be used to indicate the class of encounter (TODO://Based on FHIR value set--http://....).
| Name | Type | Description |
|---|---|---|
| ambulatory |
string |
The term ambulatory usually implies that the patient has come to the location and is not assigned to a bed. Sometimes referred to as an outpatient encounter. |
| emergency |
string |
A patient encounter that takes place at a dedicated healthcare service delivery location where the patient receives immediate evaluation and treatment, provided until the patient can be discharged or responsibility for the patient's care is transferred elsewhere (for example, the patient could be admitted as an inpatient or transferred to another facility. |
| healthHome |
string |
Healthcare encounter that takes place in the residence of the patient or a designee |
| inpatient |
string |
A patient encounter where a patient is admitted by a hospital or equivalent facility, assigned to a location where patients generally stay at least overnight and provided with room, board, and continuous nursing service. |
| observation |
string |
An encounter where the patient usually will start in different encounter, such as one in the emergency department but then transition to this type of encounter because they require a significant period of treatment and monitoring to determine whether or not their condition warrants an inpatient admission or discharge. |
| virtual |
string |
A patient encounter where the patient is not physically present for the encounter, such as in a telehealth encounter, phone call, or electronic communication. |
Fhir.R4.Annotation
A text note which also contains information about who made the statement and when Based on FHIR Annotation
| Name | Type | Description |
|---|---|---|
| authorString |
string |
Individual responsible for the annotation |
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| text |
string |
The annotation - text content (as markdown) |
| time |
string |
When the annotation was made |
Fhir.R4.CodeableConcept
Concept - reference to a terminology or just text Based on FHIR CodeableConcept
| Name | Type | Description |
|---|---|---|
| coding |
Code defined by a terminology system |
|
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| text |
string |
Plain text representation of the concept |
Fhir.R4.Coding
A Coding is a representation of a defined concept using a symbol from a defined "code system". Based on FHIR Coding
| Name | Type | Description |
|---|---|---|
| code |
string |
Symbol in syntax defined by the system |
| display |
string |
Representation defined by the system |
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| system |
string |
Identity of the terminology system |
| version |
string |
Version of the system - if relevant |
Fhir.R4.ContactDetail
Contact details (See: https://www.hl7.org/fhir/R4/metadatatypes.html#ContactDetail)
| Name | Type | Description |
|---|---|---|
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| name |
string |
Name of an individual to contact |
| telecom |
Contact details for individual or organization |
Fhir.R4.ContactPoint
Details for all kinds of technology mediated contact points for a person or organization, including telephone, email, etc. See https://www.hl7.org/fhir/R4/datatypes.html#ContactPoint
| Name | Type | Description |
|---|---|---|
| period |
Time period when the contact point was/is in use |
|
| rank |
integer |
Specify preferred order of use (1 = highest) |
| system |
phone | fax | email | pager | url | sms | other |
|
| use |
home | work | temp | old | mobile - purpose of this contact point |
|
| value |
string |
The actual contact point details |
Fhir.R4.Extension
Base for all elements Based on FHIR Element
| Name | Type | Description |
|---|---|---|
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| url |
string |
Source of the definition for the extension code - a logical name or a URL. |
| valueBoolean |
boolean |
Value as boolean |
| valueCodeableConcept |
Value as CodeableConcept |
|
| valueDateTime |
string |
Value as dateTime. |
| valueInteger |
integer |
Value as integer |
| valuePeriod |
Value as Period. |
|
| valueQuantity |
Value as Quantity |
|
| valueRange |
Value as Range. |
|
| valueRatio |
Value as Ratio. |
|
| valueReference |
Value as reference. |
|
| valueSampledData |
Value as SampledData. |
|
| valueString |
string |
Value as string |
| valueTime |
string |
Value as time (hh:mm:ss) |
Fhir.R4.Identifier
An identifier intended for computation Based on FHIR Identifier
| Name | Type | Description |
|---|---|---|
| assigner |
Organization that issued id (may be just text) |
|
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| period |
Time period when id is/was valid for use |
|
| system |
string |
The namespace for the identifier value |
| type |
Description of identifier |
|
| use |
string |
usual | official | temp | secondary | old (If known) |
| value |
string |
The value that is unique |
Fhir.R4.Meta
Metadata about a resource Based on FHIR Meta
| Name | Type | Description |
|---|---|---|
| lastUpdated |
string |
When the resource last changed - e.g. when the version changed. |
| profile |
string[] |
A list of profiles (references to StructureDefinition resources) that this resource claims to conform to. The URL is a reference to StructureDefinition.url. |
| security |
Security labels applied to this resource. These tags connect specific resources to the overall security policy and infrastructure. |
|
| source |
string |
A uri that identifies the source system of the resource. This provides a minimal amount of Provenance information that can be used to track or differentiate the source of information in the resource. The source may identify another FHIR server, document, message, database, etc. |
| tag |
Tags applied to this resource. Tags are intended to be used to identify and relate resources to process and workflow, and applications are not required to consider the tags when interpreting the meaning of a resource. |
|
| versionId |
string |
The version specific identifier, as it appears in the version portion of the URL. This value changes when the resource is created, updated, or deleted. |
Fhir.R4.Narrative
Any resource that is a DomainResource may include a human-readable narrative that contains a summary of the resource and may be used to represent the content of the resource to a human. Based on FHIR Narrative
| Name | Type | Description |
|---|---|---|
| div |
string |
xhtml |
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| status |
string |
generated, extensions, additional, empty |
Fhir.R4.Period
A time period defined by a start and end date and optionally time Based on FHIR Period
| Name | Type | Description |
|---|---|---|
| end |
string |
End time with inclusive boundary, if not ongoing |
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| start |
string |
Starting time with inclusive boundary |
Fhir.R4.Quantity
A measured or measurable amount Based on FHIR Quantity
| Name | Type | Description |
|---|---|---|
| code |
string |
Coded form of the unit |
| comparator |
string |
< | <= | >= | > - how to understand the value |
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| system |
string |
System that defines coded unit form |
| unit |
string |
Unit representation |
| value |
number |
Numerical value (with implicit precision) |
Fhir.R4.Range
A set of ordered Quantities defined by a low and high limit Based on FHIR Range
| Name | Type | Description |
|---|---|---|
| extension |
Additional Content defined by implementations |
|
| high |
High limit |
|
| id |
string |
Unique id for inter-element referencing |
| low |
Low limit |
Fhir.R4.Ratio
A ratio of two Quantity values - a numerator and a denominator Based on FHIR Ratio
| Name | Type | Description |
|---|---|---|
| denominator |
Denominator value |
|
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| numerator |
Numerator value |
Fhir.R4.Reference
A reference from one resource to another Based on FHIR Reference
| Name | Type | Description |
|---|---|---|
| display |
string |
Text alternative for the resource |
| extension |
Additional Content defined by implementations |
|
| id |
string |
Unique id for inter-element referencing |
| identifier |
Logical reference, when literal reference is not known |
|
| reference |
string |
Literal reference, Relative, internal or absolute URL |
| type |
string |
Type the reference refers to (e.g. "Patient") |
Fhir.R4.ResearchStudy
Detailed information about Research Study Based on FHIR ResearchStudy
| Name | Type | Description |
|---|---|---|
| arm |
Arm[] |
Defined path through the study for a subject |
| category |
Classifications for the study |
|
| condition |
Condition being studied |
|
| contact |
Contact details for the study |
|
| contained |
Contained, inline Resources |
|
| description |
string |
What this is study doing |
| enrollment |
Inclusion & exclusion criteria |
|
| extension |
Additional Content defined by implementations |
|
| focus |
Drugs, devices, etc. under study |
|
| id |
string |
Resource Id |
| identifier |
Business Identifier for study |
|
| implicitRules |
string |
A set of rules under which this content was created |
| keyword |
Used to search for the study |
|
| language |
string |
Language of the resource content |
| location |
Geographic region(s) for study |
|
| meta |
Metadata about the resource |
|
| modifierExtension |
Extensions that cannot be ignored |
|
| note |
Comments made about the study |
|
| objective |
A goal for the study |
|
| partOf |
Part of larger study |
|
| period |
When the study began and ended |
|
| phase |
n-a | early-phase-1 | phase-1 | phase-1-phase-2 | phase-2 | phase-2-phase-3 | phase-3 | phase-4 |
|
| primaryPurposeType |
treatment | prevention | diagnostic | supportive-care | screening | health-services-research | basic-science | device-feasibility |
|
| principalInvestigator |
Researcher who oversees multiple aspects of the study |
|
| protocol |
Steps followed in executing study |
|
| reasonStopped |
accrual-goal-met | closed-due-to-toxicity | closed-due-to-lack-of-study-progress | temporarily-closed-per-study-design |
|
| resourceType |
string:
Research |
Discriminator property for DomainResource. |
| site |
Facility where study activities are conducted |
|
| sponsor |
Organization that initiates and is legally responsible for the study |
|
| status |
active | administratively-completed | approved | closed-to-accrual | closed-to-accrual-and-intervention | completed | disapproved | in-review | temporarily-closed-to-accrual | temporarily-closed-to-accrual-and-intervention | withdrawn |
|
| text |
Text summary of the resource, for human interpretation |
|
| title |
string |
Name for this study |
Fhir.R4.Resource
Resource is the ancestor of DomainResource from which most resources are derived. Bundle, Parameters, and Binary extend Resource directly. Based on [FHIR Resource](https://www.hl7.org/fhir/r4/resource.html
| Name | Type | Description |
|---|---|---|
| id |
string |
Resource Id |
| implicitRules |
string |
A set of rules under which this content was created |
| language |
string |
Language of the resource content |
| meta |
Metadata about the resource |
|
| resourceType |
string |
The type of resource |
Fhir.R4.SampledData
A series of measurements taken by a device Based on FHIR SampledData
| Name | Type | Description |
|---|---|---|
| data |
string |
Decimal values with spaces, or "E" | "U" | "L" |
| dimensions |
integer |
Number of sample points at each time point |
| extension |
Additional Content defined by implementations |
|
| factor |
number |
Multiply data by this before adding to origin |
| id |
string |
Unique id for inter-element referencing |
| lowerLimit |
number |
Lower limit of detection |
| origin |
Zero value and units |
|
| period |
number |
Number of milliseconds between samples |
| upperLimit |
number |
Upper limit of detection |
GeographicArea
A geographic area, expressed as a Circle geometry represented using a GeoJSON Feature (see GeoJSON spec).
| Name | Type | Description |
|---|---|---|
| geometry |
|
|
| properties |
|
|
| type |
|
GeographicLocation
A location given as a combination of city, state and country/region. It could specify a city, a state or a country/region. In case a city is specified, either state +country/region or country/region (for countries/regions where there are no states) should be added. In case a state is specified (without a city), country/region should be added.
| Name | Type | Description |
|---|---|---|
| city |
string |
City name. |
| countryOrRegion |
string |
Country/region name. |
| state |
string |
State name. |
GeoJsonGeometryType
GeoJSON geometry type.
| Name | Type | Description |
|---|---|---|
| Point |
string |
GeoJsonPropertiesSubType
GeoJSON object sub-type.
| Name | Type | Description |
|---|---|---|
| Circle |
string |
GeoJsonType
GeoJSON type.
| Name | Type | Description |
|---|---|---|
| Feature |
string |
Objective
A goal for the study
| Name | Type | Description |
|---|---|---|
| name |
string |
Label for the objective |
| type |
primary | secondary | exploratory |
OrderedProcedure
Procedure information
| Name | Type | Description |
|---|---|---|
| code |
Procedure code |
|
| description |
string |
Procedure description |
| extension |
Additional Content defined by implementations |
PatientDocument
A clinical document related to a patient. Document here is in the wide sense - not just a text document (note).
| Name | Type | Description |
|---|---|---|
| administrativeMetadata |
Administrative metadata for the document. |
|
| authors |
Document author(s) |
|
| clinicalType |
The type of the clinical document. |
|
| content |
The content of the patient document. |
|
| createdDateTime |
string |
The date and time when the document was created. |
| id |
string |
A given identifier for the document. Has to be unique across all documents for a single patient. |
| language |
string |
A 2 letter ISO 639-1 representation of the language of the document. |
| specialtyType |
specialty type the document |
|
| type |
The type of the patient document, such as 'note' (text document) or 'fhirBundle' (FHIR JSON document). |
PatientInfo
Patient structured information, including demographics and known structured clinical information.
| Name | Type | Description |
|---|---|---|
| birthDate |
string |
The patient's date of birth. |
| clinicalInfo |
Known clinical information for the patient, structured. |
|
| sex |
The patient's sex. |
PatientInfoSex
The patient's sex.
| Name | Type | Description |
|---|---|---|
| female |
string |
|
| male |
string |
|
| unspecified |
string |
PatientRecord
A patient record, including their clinical information and data.
| Name | Type | Description |
|---|---|---|
| encounters |
Patient encounters/visits. |
|
| id |
string |
A given identifier for the patient. Has to be unique across all patients in a single request. |
| info |
Patient structured information, including demographics and known structured clinical information. |
|
| patientDocuments |
Patient unstructured clinical data, given as documents. |
ResearchStudyStatusCodeType
active | administratively-completed | approved | closed-to-accrual | closed-to-accrual-and-intervention | completed | disapproved | in-review | temporarily-closed-to-accrual | temporarily-closed-to-accrual-and-intervention | withdrawn
| Name | Type | Description |
|---|---|---|
| active |
string |
The study is open for accrual. |
| administratively-completed |
string |
Study is completed prematurely and will not resume; patients are no longer examined nor treated. |
| approved |
string |
Protocol is approved by the review board. |
| closed-to-accrual |
string |
Study is closed for accrual; patients can be examined and treated. |
| closed-to-accrual-and-intervention |
string |
The study is closed to accrual and intervention, i.e. the study is closed to enrollment, all study subjects have completed treatment or intervention but are still being followed according to the primary objective of the study. |
| completed |
string |
Study is closed to accrual and intervention, i.e. the study is closed to enrollment, all study subjects have completed treatment or intervention but are still being followed according to the primary objective of the study. |
| disapproved |
string |
Protocol was disapproved by the review board. |
| in-review |
string |
Protocol is submitted to the review board for approval. |
| temporarily-closed-to-accrual |
string |
The study is temporarily closed to accrual; a pause in accrual while study is reviewed, but is expected to resume. |
| temporarily-closed-to-accrual-and-intervention |
string |
Study is temporarily closed for accrual; can be potentially resumed in the future |
| withdrawn |
string |
Protocol was withdrawn by the lead organization. |
SpecialtyType
Known values codes that can be used to indicate the type of the Specialty.
| Name | Type | Description |
|---|---|---|
| pathology |
string |
pathology |
| radiology |
string |
radiology |
TimePeriod
A duration of time during which an event is happening
| Name | Type | Description |
|---|---|---|
| end |
string |
End time with inclusive boundary, if not ongoing |
| start |
string |
Starting time with inclusive boundary |
TrialMatcherData
The body of the Trial Matcher request.
| Name | Type | Description |
|---|---|---|
| configuration |
Configuration affecting the Trial Matcher model's inference. |
|
| patients |
The list of patients, including their clinical information and data. |
TrialMatcherModelConfiguration
Configuration affecting the Trial Matcher model's inference.
| Name | Type | Default value | Description |
|---|---|---|---|
| clinicalTrials |
The clinical trials that the patient(s) should be matched to. |
||
| includeEvidence |
boolean |
True |
An indication whether the model's output should include evidence for the inferences. |
| verbose |
boolean |
False |
An indication whether the model should produce verbose output. |