Clinical trial
REPRISE EDGE: REpositionable Percutaneous Replacement of NatIve StEnotic Aortic Valve Through Implantation of LOTUS EDGE Valve System - Evaluation of Performance and Safety
NCT02854319 is registered in ClinicalTrials.gov with Boston Scientific Corporation as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- REPRISE EDGE: REpositionable Percutaneous Replacement of NatIve StEnotic Aortic Valve Through Implantation of LOTUS EDGE Valve System - Evaluation of Performance and Safety
- Lead sponsor
- Boston Scientific Corporation
- Phase
- Not applicable
- Overall status
- Terminated
- Start date
- September 7, 2016
- Completion date
- March 13, 2018
- Enrollment
- 15 (actual)
- Sites
- 3
Conditions
As the registry lists them; a condition with its own page is linked.