REPRISE EDGE 29 mm EU Study

Status Withdrawn

Clinical Trial Summary

The objective of the REPRISE EDGE 29 mm EU study is to evaluate performance and safety of the 29 mm 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 aortic valve replacement (SAVR).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Aortic Valve Stenosis

Clinical Trial Details

NCT number	NCT02964962
Study type	Interventional
Source	Boston Scientific Corporation
Contact
Status	Withdrawn
Phase	N/A
Start date	April 1, 2018
Completion date	December 30, 2018

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See also
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