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ACTIVE NOT RECRUITING
NCT03230747
NA

SAPIEN M3 EFS: Early Feasibility Study of the Edwards SAPIEN M3 System for the Treatment of Mitral Regurgitation

Sponsor: Edwards Lifesciences

View on ClinicalTrials.gov

Summary

This study will evaluate the safety and functionality of the SAPIEN M3 System in patients with symptomatic, severe MR and will provide guidance for future clinical study designs utilizing the SAPIEN M3 System.

Official title: Early Feasibility Study of the Edwards SAPIEN M3 System for the Treatment of Mitral Regurgitation

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

72

Start Date

2017-09-14

Completion Date

2027-08

Last Updated

2025-07-22

Healthy Volunteers

No

Interventions

DEVICE

Edwards SAPIEN M3 System

SAPIEN M3 System includes the SAPIEN M3 valve and the SAPIEN M3 dock

Locations (9)

Cedars-Sinai Medical Center Heart Institute

Los Angeles, California, United States

California Pacific Medical Center

San Francisco, California, United States

Emory University

Atlanta, Georgia, United States

Evanston/ Northshore University

Evanston, Illinois, United States

Henry Ford Hospital

Detroit, Michigan, United States

Mayo Clinic

Rochester, Minnesota, United States

Intermountain Medical Center

Murray, Utah, United States

Sentara Cardiovascular Research Institution

Norfolk, Virginia, United States

St. Paul's Hospital

Vancouver, British Columbia, Canada