Innoventric Trillium™ Stent Graft Early Feasibility Study (EFS)
Start Date
8/5/2024
Completion Date
8/1/2030
Summary
Early Feasibility Study to evaluate the safety and performance of the Innoventric Trillium™ Stent Graft in the treatment of severe or greater tricuspid regurgitation (TR).
Detailed Description
Prospective, single arm, multi-center, Early Feasibility Study (EFS) to assess the safety and performance of the Innoventric Trillium™ Stent Graft in the treatment of severe or greater tricuspid regurgitation (TR). Up to fifteen (15) patients at up to 10 US investigational sites and 3 German investigational sites will be enrolled. All enrolled study patients will be assessed at baseline, during the procedure, at discharge, and after 1 month, 3 months, 6 months, 1 year, 2 years, 3 years, 4 years, and 5 years following the index procedure.
Eligibility Criteria
Age Range: 18 years to 85 years
Interventions
Trillium™
Conditions
Locations
Cardiovascular Institute of Los Robles Health System
Thousand Oaks, California 91360
United States
Ascension St. John
Detroit, Michigan 48236
United States
Mayo Clinic Hospital (Rochester)
Rochester, Minnesota 55902
United States
Weill Cornell Medicine
New York, New York 10065
United States
Stony Brook Heart Institute
Stony Brook, New York 11794
United States
The Christ Hospital
Cincinnati, Ohio 45219
United States
Lankenau Heart Institute
Philadelphia, Pennsylvania 19096
United States
TriStar Centennial Medical Center
Nashville, Tennessee 37203
United States
University of Washington Medical Center
Seattle, Washington 98195
United States
University Medicine Mainz
Mainz, Rhineland-Palatinate 55131
Germany
Helios Health Institute GmbH, Leipzig
Leipzig, Saxony 04103
Germany
German Heart Center at Charité (DHZC)
Berlin, State of Berlin 13353
Germany