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Safety and Efficacy Study of Lotus Valve for Transcatheter Aortic Valve Replacement — REPRISE III  

Aortic Stenosis Clinical Trial

Official title:
REPRISE III: Repositionable Percutaneous Replacement of Stenotic Aortic Valve Through Implantation of Lotus™ Valve System - Randomized Clinical Evaluation

Clinical Trial Summary

The objective of this study is to evaluate the safety and effectiveness of the Lotus™ Valve System and LOTUS Edge™ Valve System for transcatheter aortic valve replacement (TAVR) in symptomatic subjects with calcific, severe native aortic stenosis who are considered at extreme or high risk for surgical valve replacement.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02202434
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Terminated
Phase N/A
Start date September 22, 2014
Completion date May 21, 2021
View Details
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