Cephea Early Feasibility Study
Abbott Medical Devices
Summary
The objective of this study is to evaluate the preliminary safety and effectiveness of the Cephea Mitral Valve System for the treatment of symptomatic patients with mitral valve disease (including mitral regurgitation, mitral stenosis and mixed mitral valve disease) in whom transcatheter therapy is deemed more appropriate than open heart surgery.
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
Key Inclusion Criteria: * Mitral valve disease resulting in mitral regurgitation (MR ≥ Grade III) and/or severe mitral valve stenosis (mitral valve area ≤ 1.5cm²) per American Society of Echocardiography criteria. * LVEF ≥ 30% * In the judgement of the Site Heart Team, transcatheter therapy is deemed more appropriate than open heart surgery. Key Exclusion Criteria: * Prior surgical or interventional treatment that interferes with the Cephea valve delivery or function. * Need for emergent or urgent surgery.
Interventions
- DeviceCephea Mitral Valve System
Transcatheter mitral valve replacement
Locations (22)
- Banner-University Medical Center PhoenixPhoenix, Arizona
- Cedars-Sinai Medical CenterLos Angeles, California
- University of California - Davis Medical CenterSacramento, California
- Los Robles Regional Medical CenterThousand Oaks, California
- Emory University HospitalAtlanta, Georgia
- Piedmont Heart InstituteAtlanta, Georgia