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Beating Heart Mitral Valve Repair With the HARPOON™ System — RESTORE  

Mitral Regurgitation Clinical Trial

Official title:
A Prospective, Multi-center Trial to Evaluate the Safety and Effectiveness of Beating Heart Mitral Valve Repair With the HARPOON™ System (RESTORE)

Clinical Trial Summary

The objective of the study is to evaluate the safety and effectiveness of the HARPOON™ System in the treatment of patients with severe degenerative mitral regurgitation (DMR).

Clinical Trial Description

RESTORE is a prospective, multicenter, non-randomized trial designed to evaluate the safety and effectiveness of the HARPOON™ Beating Heart Mitral Valve Repair System in patients with severe degenerative mitral regurgitation (DMR). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04375332
Study type Interventional
Source Edwards Lifesciences
Contact
Status Active, not recruiting
Phase N/A
Start date December 16, 2020
Completion date December 2027
View Details
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