RecruitingNCT04890821
Early Feasibility Study of the Cardiac Implants Percutaneous Ring Annuloplasty System
AI Description
An early feasibility study to evaluate the safety and performance of 1) the transcatheter delivery and implantation of the Cardiac Implants (CI) annuloplasty ring and 2) the adjustment of the ring approximately 90 days following implantation in patients suffering from ≥ moderate functional tricuspid regurgitation (FTR).
- Who can join
- adult, older adult
- Participants
- 15
- Expected completion
- 2027-09
- Funded by
- industry
Conditions studied
Tricuspid Regurgitation Functional
What is being tested
- DEVICE: CI Percutaneous Ring Annuloplasty System
What it measures
- Freedom from device or procedure-related mortality, Freedom from mortality determined to be primarily caused by the device or procedure in the primary endpoint cohort. Events adjudicated by a Clinical Events Committee (CEC)., 30 days post-adjustment
Centers Participating
These centers are participating in this study. Reach out to them directly to learn more.
Registry entry updated 2021-11-30
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.