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Clinical Trial Summary

The purpose of this study is to collect clinical evidence on valve performance and procedural outcomes associated with an "optimized" TAVR care pathway and post-TAVR conduction disturbance pathway while using the Evolut™ PRO and Evolut™ PRO+ devices. The purpose of the addendum is to collect post-market clinical evidence on valve performance and procedural outcomes associated with the Evolut FX Device.


Clinical Trial Description

This is a post market, multi-center (sites in US/CAN/EMEA/ANZ), prospective, non-randomized study. The addendum is a post market, multi-center (sites in US only), prospective, non-randomized study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04091048
Study type Observational
Source Medtronic Cardiovascular
Contact
Status Active, not recruiting
Phase
Start date September 16, 2019
Completion date December 2024

See also
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