HAART Annuloplasty Device Valve Repair Registry
NCT04035356 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 183
Last updated 2024-08-09
Summary
Multicenter US registry study to assess procedure success and long-term (10-year) performance of the HAART 200 and HAART 300 Aortic Annuloplasty Devices when used during aortic valve repair in a routine cardiovascular practice setting.
Conditions
- Aortic Valve Insufficiency
- Aortic Aneurysm
Interventions
- DEVICE
-
Aortic valve repair
Use of a HAART Aortic Annuloplasty Device in patients undergoing aortic valve repair surgery
Sponsors & Collaborators
-
Biostable Science & Engineering
lead INDUSTRY
Principal Investigators
-
J. Scott Rankin, MD · West Virginia University Heart and Vascular Institute
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-09-22
- Primary Completion
- 2024-07-25
- Completion
- 2024-07-25
- FDA Device
- Yes
Countries
- United States
Study Locations
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