Clinical TrialID 5537
Anticoagulation for Aortic Bioprosthesis (ANTIPRO)
NCT03807921
Aortic Valve Stenosis|Aortic Valve Disease|Aortic Valve Insufficiency|Aortic Valve Regurgitation
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 5537
- Evidence Id
- 5537
- Core Evidence Id
- 5537
- Source Clinical Trial Id
- 5519
- Herb2 Clinical Trial Id
- HBCT005519
- Nct Id
- NCT03807921
- Title
- Anticoagulation for Aortic Bioprosthesis (ANTIPRO)
- Status
- Completed
- Phase
- Phase 4
- Study Result
- No
- Study Condition
- Aortic Valve Stenosis|Aortic Valve Disease|Aortic Valve Insufficiency|Aortic Valve Regurgitation
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
- Intervention
- DRUG: Warfarin|DRUG: Aspirin
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Single
- Intervention Purpose
- Treatment
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 140
- Outcome Measure
- Transprosthetic aortic gradient, Change in Transprosthetic mean gradient, 3 months and 1 year|Change in New York Heart Association (NYHA) class, NYHA class, 1 year
- Sponsor Collaborator
- Instituto Nacional de Cirugia Cardiaca, Uruguay|Universidad de la Republica
- Funded By
- OTHER
- Location
- Centro Cardiovascular Universitario, Montevideo, Uruguay|Instituto Nacional de Cirugia Cardiaca, Montevideo, Uruguay
- Other Id
- ANTIPRO
- Start Date
- 2019-01-01
- Primary Completion Date
- 2019-12-30
- Completion Date
- 2019-12-31
- First Posted
- 2019-01-17
- Results First Posted
- Last Update Posted
- 2022-03-08
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT03807921
- Title Cn
- Title En
- Anticoagulation for Aortic Bioprosthesis (ANTIPRO)
- Bilingual Status
- semi_complete