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Clinical Trial Summary

Obtain safety and effectiveness data to support indication expansion for the Medtronic TAVR System to include patients with moderate, AS.


Clinical Trial Description

Multi-center, international, prospective, randomized study. Subjects will be randomized to either transcatheter aortic valve replacement (TAVR) with the Evolut PRO+ TAVR System, or Evolut FX System, and guideline-directed management (GDMT) or GDMT alone. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05149755
Study type Interventional
Source Medtronic Cardiovascular
Contact Hang Nguyen
Phone +1765262832
Email hang.t.nguyen@medtronic.com
Status Recruiting
Phase N/A
Start date April 27, 2022
Completion date December 2034