Beating Heart Mitral Valve Repair With the HARPOON™ System
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
Summary
- Conditions
- Mitral Regurgitation
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment
Participation Requirements
- Age
- Between 21 years and 125 years
- Gender
- Both males and females
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).
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).
Tracking Information
- NCT #
- NCT04375332
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Vinod H. Thourani, MD Dept of Cardiovascular Surgery, Piedmont Heart Institute Principal Investigator: Konstantinos Koulogiannis, MD Department of Cardiovascular Medicine Gagnon Cardiovascular Institute
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