FHIR IG analytics| Package | hl7.fhir.uv.ebm |
| Resource Type | Composition |
| Id | Composition-370502.json |
| FHIR Version | R6 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
Generated Narrative: Composition 370502
version: 25; Last updated: 2025-10-21 10:47:22+0000; Language: en
Profile: ParticipantFlowReport
ArtifactPublicationStatus: Active
url: https://fevir.net/resources/Composition/370502
identifier: FEvIR Object Identifier/370502, FEvIR Linking Identifier/NCT03640312-participant-flow-report
status: Final
type: Participant Flow Report
date: 2025-10-21 10:47:22+0000
author: [No author listed.]
title: Participant Flow Report for NCT03640312
custodian: Computable Publishing LLC
| Type | Target[x] |
| Cite As | Participant Flow Report for NCT03640312 [Database Entry: FHIR Composition Resource]. Contributors: [No author listed.] [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 370502. Revised 2025-10-21. Available at: https://fevir.net/resources/Composition/370502. Computable resource at: https://fevir.net/resources/Composition/370502#json. |
Generated Narrative: Group #FG000
Profile: ExposureGroup
name: NCT03640312 Flow Group QUARTET LDQT
description:
Patients randomized to the intervention arm took a once daily ultra-low-dose quadruple combination therapy (QUARTET LDQT). The LDQT is an overencapsulated combination pill comprising four types of blood pressure lowering medications each at ¼ standard doses. QUARTET includes candesartan 2mg, amlodipine besylate 1.25mg, indapamide 0.625mg, and bisoprolol 2.5mg. The individual components are currently approved and marketed within the United States.
QUARTET LDQT: Ultra-low-dose combination therapy comprising four different blood pressure lowering drugs at 1/4 dosages. Taken once daily for 12 weeks.
type: Person
membership: Enumerated
quantity: 32
Characteristics
Code Value[x] Exclude Research Study from which this is a flow group NCT03640312 false
Generated Narrative: Group #FG001
Profile: ExposureGroup
name: NCT03640312 Flow Group Candesartan
description:
Patients randomized to the comparison arm took a once daily 8mg candesartan.
Candesartan: Standard monotherapy of 8mg candesartan. Taken once daily for 12 weeks.
type: Person
membership: Enumerated
quantity: 30
Characteristics
Code Value[x] Exclude Research Study from which this is a flow group NCT03640312 false
Generated Narrative: Evidence #NCT03640312-flow-milestone-0-Overall-Study-group-FG000
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-0-Overall-Study-group-FG000
title: ParticipantFlowEvidence: NCT03640312 QUARTET LDQT - STARTED at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: QUARTET LDQT
variableDefinition
variableRole: Outcome
observed: STARTED at Overall Study
Statistics
StatisticType Quantity Count 32
Generated Narrative: Evidence #NCT03640312-flow-milestone-0-Overall-Study-group-FG001
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-0-Overall-Study-group-FG001
title: ParticipantFlowEvidence: NCT03640312 Candesartan - STARTED at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: Candesartan
variableDefinition
variableRole: Outcome
observed: STARTED at Overall Study
Statistics
StatisticType Quantity Count 30
Generated Narrative: Evidence #NCT03640312-flow-milestone-1-Overall-Study-group-FG000
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-1-Overall-Study-group-FG000
title: ParticipantFlowEvidence: NCT03640312 QUARTET LDQT - 6 Week Follow Up at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: QUARTET LDQT
variableDefinition
variableRole: Outcome
observed: 6 Week Follow Up at Overall Study
Statistics
StatisticType Quantity Count 32
Generated Narrative: Evidence #NCT03640312-flow-milestone-1-Overall-Study-group-FG001
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-1-Overall-Study-group-FG001
title: ParticipantFlowEvidence: NCT03640312 Candesartan - 6 Week Follow Up at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: Candesartan
variableDefinition
variableRole: Outcome
observed: 6 Week Follow Up at Overall Study
Statistics
StatisticType Quantity Count 28
Generated Narrative: Evidence #NCT03640312-flow-milestone-2-Overall-Study-group-FG000
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-2-Overall-Study-group-FG000
title: ParticipantFlowEvidence: NCT03640312 QUARTET LDQT - COMPLETED at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: QUARTET LDQT
variableDefinition
variableRole: Outcome
observed: COMPLETED at Overall Study
Statistics
StatisticType Quantity Count 29
Generated Narrative: Evidence #NCT03640312-flow-milestone-2-Overall-Study-group-FG001
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-2-Overall-Study-group-FG001
title: ParticipantFlowEvidence: NCT03640312 Candesartan - COMPLETED at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: Candesartan
variableDefinition
variableRole: Outcome
observed: COMPLETED at Overall Study
Statistics
StatisticType Quantity Count 24
Generated Narrative: Evidence #NCT03640312-flow-milestone-3-Overall-Study-group-FG000
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-3-Overall-Study-group-FG000
title: ParticipantFlowEvidence: NCT03640312 QUARTET LDQT - NOT COMPLETED at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: QUARTET LDQT
variableDefinition
variableRole: Outcome
observed: NOT COMPLETED at Overall Study
Statistics
StatisticType Quantity Count 3
Generated Narrative: Evidence #NCT03640312-flow-milestone-3-Overall-Study-group-FG001
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-milestone-3-Overall-Study-group-FG001
title: ParticipantFlowEvidence: NCT03640312 Candesartan - NOT COMPLETED at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: Candesartan
variableDefinition
variableRole: Outcome
observed: NOT COMPLETED at Overall Study
Statistics
StatisticType Quantity Count 6
Generated Narrative: Evidence #NCT03640312-flow-reason-Overall-Study-group-FG000
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-reason-Overall-Study-group-FG000
title: ParticipantFlowEvidence: NCT03640312 QUARTET LDQT - Reasons for withdraw at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: QUARTET LDQT
variableDefinition
variableRole: Outcome
observed: Reasons for withdraw at Overall Study
Statistics
StatisticType Category Quantity Count Lost to Follow-up 3
Generated Narrative: Evidence #NCT03640312-flow-reason-Overall-Study-group-FG001
Profile: ParticipantFlowEvidence
identifier: FEvIR Linking Identifier/NCT03640312-flow-reason-Overall-Study-group-FG001
title: ParticipantFlowEvidence: NCT03640312 Candesartan - Reasons for withdraw at Overall Study
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
UseContexts
Code Value[x] Evidence Based Medicine on FHIR Implementation Guide Code System: evidence-communication (Evidence Communication) ParticipantFlowEvidence variableDefinition
variableRole: Population
observed: Candesartan
variableDefinition
variableRole: Outcome
observed: Reasons for withdraw at Overall Study
Statistics
StatisticType Category Quantity Count Lost to Follow-up 6
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