Active, not recruitingNCT07116551
Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System for the Treatment of Severe, Symptomatic Aortic Stenosis
AI Description
The purpose of this study is to evaluate the safety and functionality of Abbott's BE TAVI system for the treatment of patients with symptomatic severe aortic valve stenosis.
- Who can join
- adult, older adult
- Participants
- 11
- Expected completion
- 2031-06
- Funded by
- industry
Conditions studied
Symptomatic Severe Aortic Stenosis
What is being tested
- DEVICE: Abbott BE TAVI System
What it measures
- Device success, Intended performance of the valve, 30 days
- Technical success, Successful access, delivery of the Abbott BE TAVI valve, and retrieval of the delivery system., From start of procedure up to end of procedure
Centers Participating
These centers are participating in this study. Reach out to them directly to learn more.
Registry entry updated 2026-02-06
Deciding whether to join a study is your choice, and you can ask a study team questions before you decide anything.
If you would rather we did it with you, call us on (656) 206-4686.