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Study identifier: NCT04890821 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Early Feasibility Study of the Cardiac Implants Percutaneous Ring Annuloplasty System

Condition: Tricuspid Regurgitation Functional  ·  Sponsor: Cardiac Implants LLC

PhaseNA
Planned participants15
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

Nodar Kipshidze, MPH  ·  1-917-370-6247  ·  Nodar@cardiac-implants.com

Always discuss trial participation with your own doctor first.

Locations (2)

Hackensack University Medical CenterHackensack, New Jersey, United StatesNot Yet Recruiting
Weill Cornell Medicine-New York Presbyterian HospitalNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04890821