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Clinical Trial Summary

The purpose of the study is to obtain safety and effectiveness data of the Medtronic Evolut™ PRO+ TAVR System for the treatment of severe, asymptomatic aortic stenosis.


Clinical Trial Description

Single-arm, descriptive, multi-center, international All subjects will be treated with a Medtronic Evolut™ PRO+ TAVR System. Subject follow-ups will be conducted at pre and post-procedure, discharge, 30 days, 6 months, and annually through 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04639258
Study type Interventional
Source Medtronic Cardiovascular
Contact
Status Terminated
Phase N/A
Start date May 28, 2021
Completion date June 7, 2022

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