Status: Recruiting
Early Feasibility Study of the Cardiac Implants Percutaneous Ring Annuloplasty System
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).
Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Cardiac Implants LLCUpdated: Nov 30, 2021Locations: 2
Eligibility criteria
Moderate to severe functional tricuspid regurgitation (TR) defined by ASE guidel... [+9]
Acute decompensated heart failure requiring hospital admission with 4 weeks of e... [+30]