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SAPIEN M3 EFS: Early Feasibility Study of the Edwards SAPIEN M3 System for the Treatment of Mitral Regurgitation
Sponsor: Edwards Lifesciences
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
Conditions
Interventions
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