FHIR IG analytics| Package | hl7.fhir.uv.ebm |
| Resource Type | Evidence |
| Id | Evidence-267237.json |
| FHIR Version | R6 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
Generated Narrative: Evidence 267237
version: 9; Last updated: 2025-12-11 20:35:21+0000; Language: en
Profile: NonComparativeEvidence
url: https://fevir.net/resources/Evidence/267237
identifier: FEvIR Object Identifier/267237, FEvIR Linking Identifier/NCT03421379-secondaryOutcomeMeasure-1--OG001
name: NCT03421379_secondaryOutcomeMeasure_1_OG001
title: PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379
citeAs:
PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 [Database Entry: FHIR Evidence Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 267237. Revised 2025-12-11. Available at: https://fevir.net/resources/Evidence/267237. Computable resource at: https://fevir.net/resources/Evidence/267237#json.
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
publisher: Computable Publishing LLC
contact: support@computablepublishing.com
copyright:
https://creativecommons.org/licenses/by-nc-sa/4.0/
description:
This Evidence Resource is referenced in an example for the EBMonFHIR Implementation Guide.
variableDefinition
description:
Glucagon Hydrochloride Solution
note: ,
Outcome Measure Population Description: All randomized participants who received at least one dose of study drug and had evaluable PD data.
Outcome Measure Denominator Units: Participants
variableRole: Population
observed: A single dose of 1 mg glucagon hydrochloride solution was administered IM (Identifier: ClinicalTrials.gov Outcome Measurement Group Id/OG001)
variableDefinition
variableRole: Outcome
statistic
statisticType: median
quantity: 1.5 hour
SampleSizes
KnownDataCount 70 AttributeEstimates
Type Range Full Range 0.67-4 hour
{
"resourceType": "Evidence",
"id": "267237",
"meta": {
"versionId": "9",
"lastUpdated": "2025-12-11T20:35:21.032Z",
"profile": [
"http://hl7.org/fhir/uv/ebm/StructureDefinition/non-comparative-evidence"
]
},
"language": "en",
"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
},
"url": "https://fevir.net/resources/Evidence/267237",
"identifier": [
{
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/v2-0203",
"code": "ACSN",
"display": "Accession ID"
}
],
"text": "FEvIR Object Identifier"
},
"system": "https://fevir.net/FOI",
"value": "267237",
"assigner": {
"display": "Computable Publishing LLC"
}
},
{
"type": {
"text": "FEvIR Linking Identifier"
},
"system": "https://fevir.net/FLI",
"value": "NCT03421379-secondaryOutcomeMeasure-1--OG001",
"assigner": {
"display": "Computable Publishing LLC"
}
}
],
"name": "NCT03421379_secondaryOutcomeMeasure_1_OG001",
"title": "PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379",
"citeAs": "PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration for Glucagon Hydrochloride Solution in NCT03421379 [Database Entry: FHIR Evidence Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 267237. Revised 2025-12-11. Available at: https://fevir.net/resources/Evidence/267237. Computable resource at: https://fevir.net/resources/Evidence/267237#json.",
"status": "active",
"author": [
{
"name": "Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter"
}
],
"publisher": "Computable Publishing LLC",
"contact": [
{
"telecom": [
{
"system": "email",
"value": "support@computablepublishing.com"
}
]
}
],
"copyright": "https://creativecommons.org/licenses/by-nc-sa/4.0/",
"description": "This Evidence Resource is referenced in an example for the EBMonFHIR Implementation Guide.",
"variableDefinition": [
{
"description": "Glucagon Hydrochloride Solution",
"note": [
{
"text": "Outcome Measure Population Description: All randomized participants who received at least one dose of study drug and had evaluable PD data."
},
{
"text": "Outcome Measure Denominator Units: Participants"
}
],
"variableRole": "population",
"observed": {
"identifier": {
"type": {
"text": "ClinicalTrials.gov Outcome Measurement Group Id"
},
"value": "OG001"
},
"display": "A single dose of 1 mg glucagon hydrochloride solution was administered IM"
}
},
{
"variableRole": "outcome",
"observed": {
"reference": "EvidenceVariable/267228",
"type": "EvidenceVariable",
"identifier": {
"type": {
"text": "FEvIR Linking Identifier"
},
"system": "https://fevir.net/FLI",
"value": "NCT03421379-secondaryOutcome-1",
"assigner": {
"display": "Computable Publishing LLC"
}
},
"display": "PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM at Pre-dose, 5, 10, 15, 20, 25, 30, 40, 50, 60, 90, 120, 240 minutes after each glucagon administration - (NCT03421379)"
}
}
],
"statistic": [
{
"statisticType": {
"coding": [
{
"system": "https://fevir.net/sevco",
"code": "STATO:0000574",
"display": "median"
}
]
},
"quantity": {
"value": 1.5,
"unit": "hour"
},
"sampleSize": {
"knownDataCount": 70
},
"attributeEstimate": [
{
"type": {
"text": "Full Range"
},
"range": {
"low": {
"value": 0.67,
"unit": "hour"
},
"high": {
"value": 4,
"unit": "hour"
}
}
}
]
}
]
}