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Treatment of Mitral Regurgitation Using a Minimally Invasive Approach With the HARPOON Device. — ASCEND  

Mitral Regurgitation Clinical Trial

Official title:
Assessment of the Safety and Performance of the HARPOON™ Beating Heart Mitral Valve Repair System; a Multi-center Post-market Study (ASCEND)

Clinical Trial Summary

To evaluate the long-term safety and performance of the HARPOON™ MVRS for use in patients presenting with severe degenerative mitral regurgitation due to posterior leaflet prolapse in the post-market phase.

Clinical Trial Description

This trial is a single arm, prospective, multi-center, non-randomized and open-label post-market study that will evaluate subjects for up to 5 years post treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04382612
Study type Interventional
Source Edwards Lifesciences
Contact
Status Terminated
Phase N/A
Start date October 2, 2020
Completion date December 1, 2022
View Details
See also
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