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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


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

See also
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