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FHIR IG analytics

Packagehl7.fhir.uv.ebm
Resource TypeEvidence
IdEvidence-367904.json
FHIR VersionR6

Resources that use this resource

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Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: Evidence 367904

version: 26; Last updated: 2025-08-18 13:22:42+0000; Language: en

Profile: NonComparativeEvidence

ArtifactPublicationStatus: Active

url: https://fevir.net/resources/Evidence/367904

identifier: FEvIR Object Identifier/367904, FEvIR Linking Identifier/NCT03640312-primaryOutcomeMeasure-0--OG001

name: NCT03640312_primaryOutcomeMeasure_0_OG001

title: Change in Mean Systolic Blood Pressure at 12 weeks for Candesartan in NCT03640312

citeAs:

Change in Mean Systolic Blood Pressure at 12 weeks for Candesartan in NCT03640312 [Database Entry: FHIR Evidence Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 367904. Revised 2025-08-18. Available at: https://fevir.net/resources/Evidence/367904. Computable resource at: https://fevir.net/resources/Evidence/367904#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:

Candesartan

note: ,

Outcome Measure Population Description: Modified intent to treat whereby all those participants with data at any follow-up time point and baseline to contribute to analyses will be included in analyses according to arm to which they were randomized, regardless of adherence to the study protocol.

Outcome Measure Denominator Units: Participants

variableRole: Population

observed: Patients randomized to the comparison arm took a once daily 8mg candesartan. Candesartan: Standard monotherapy of 8mg candesartan. Taken once daily for 12 weeks. (Identifier: ClinicalTrials.gov Outcome Measurement Group Id/OG001)

variableDefinition

variableRole: Outcome

observed: Change in Mean Systolic Blood Pressure at 12 weeks - (NCT03640312)

statistic

statisticType: Least Squares Mean

quantity: -10.87 mm Hg

SampleSizes

-KnownDataCount
*30

AttributeEstimates

-TypeRange
*95% Confidence Interval-15.24--6.5 mm Hg

Source1

{
  "resourceType": "Evidence",
  "id": "367904",
  "meta": {
    "versionId": "26",
    "lastUpdated": "2025-08-18T13:22:42.074Z",
    "profile": [
      "http://hl7.org/fhir/uv/ebm/StructureDefinition/non-comparative-evidence"
    ]
  },
  "language": "en",
  "text": {
    "status": "extensions",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/uv/ebm/StructureDefinition/artifact-publication-status",
      "valueCodeableConcept": {
        "coding": [
          {
            "system": "http://terminology.hl7.org/CodeSystem/cited-artifact-status-type",
            "code": "active",
            "display": "Active"
          }
        ]
      }
    }
  ],
  "url": "https://fevir.net/resources/Evidence/367904",
  "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": "367904",
      "assigner": {
        "display": "Computable Publishing LLC"
      }
    },
    {
      "type": {
        "text": "FEvIR Linking Identifier"
      },
      "system": "https://fevir.net/FLI",
      "value": "NCT03640312-primaryOutcomeMeasure-0--OG001",
      "assigner": {
        "display": "Computable Publishing LLC"
      }
    }
  ],
  "name": "NCT03640312_primaryOutcomeMeasure_0_OG001",
  "title": "Change in Mean Systolic Blood Pressure at 12 weeks for Candesartan in NCT03640312",
  "citeAs": "Change in Mean Systolic Blood Pressure at 12 weeks for Candesartan in NCT03640312 [Database Entry: FHIR Evidence Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 367904. Revised 2025-08-18. Available at: https://fevir.net/resources/Evidence/367904. Computable resource at: https://fevir.net/resources/Evidence/367904#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": "Candesartan",
      "note": [
        {
          "text": "Outcome Measure Population Description: Modified intent to treat whereby all those participants with data at any follow-up time point and baseline to contribute to analyses will be included in analyses according to arm to which they were randomized, regardless of adherence to the study protocol."
        },
        {
          "text": "Outcome Measure Denominator Units: Participants"
        }
      ],
      "variableRole": "population",
      "observed": {
        "identifier": {
          "type": {
            "text": "ClinicalTrials.gov Outcome Measurement Group Id"
          },
          "value": "OG001"
        },
        "display": "Patients randomized to the comparison arm took a once daily 8mg candesartan.\n\nCandesartan: Standard monotherapy of 8mg candesartan. Taken once daily for 12 weeks."
      }
    },
    {
      "variableRole": "outcome",
      "observed": {
        "reference": "EvidenceVariable/367882",
        "type": "EvidenceVariable",
        "identifier": {
          "type": {
            "text": "FEvIR Linking Identifier"
          },
          "system": "https://fevir.net/FLI",
          "value": "NCT03640312-primaryOutcome-0",
          "assigner": {
            "display": "Computable Publishing LLC"
          }
        },
        "display": "Change in Mean Systolic Blood Pressure at 12 weeks -  (NCT03640312)"
      }
    }
  ],
  "statistic": [
    {
      "statisticType": {
        "text": "Least Squares Mean"
      },
      "quantity": {
        "value": -10.87,
        "unit": "mm Hg"
      },
      "sampleSize": {
        "knownDataCount": 30
      },
      "attributeEstimate": [
        {
          "type": {
            "text": "95% Confidence Interval"
          },
          "range": {
            "low": {
              "value": -15.24,
              "unit": "mm Hg"
            },
            "high": {
              "value": -6.5,
              "unit": "mm Hg"
            }
          }
        }
      ]
    }
  ]
}