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NCT06212193NARecruiting

Innoventric Trillium™ Stent Graft Early Feasibility Study (EFS)

Innoventric LTD

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

Inclusion Criteria: * Patient has clinically significant TR graded as severe or greater * Peak central venous pressure of ≥ 15mmHg * Patient has NYHA functional classification of III or IV * Patient is not eligible for standard-of-care surgical or interventional therapy or has refused standard-of-care surgical and interventional therapy or has received standard-of-care TR therapy and remains symptomatic Exclusion Criteria: Patients will be excluded from participation if ANY of the following criteria apply: * Severe RV dysfunction defined by TAPSE, RVEF, or RVFAC. * Anatomical suitability according to CT scan. * Systolic Pulmonary Artery Pressure \> 65mmHg * Moderate or more mitral valve stenosis * Greater than moderate mitral valve regurgitation or aortic valve stenosis/regurgitation * Moderate mitral valve regurgitation combined with moderate aortic valve stenosis/regurgitation * Kidney dysfunction with estimated Glomerular Filtration Rate (eGFR) \< 35 ml/min/1.73 m2 within 60 days prior to the index procedure or patient is on chronic dialysis * Liver cirrhosis or moderate or severe liver disease (Child-Turcotte-Pugh class B or C, or a score of 7 or higher) * Thrombocytopenia (Platelet count\< 80,000/mm3) or thrombocytosis (Platelet count \> 750,000/mm3) within 14 days of the index procedure * In the opinion of the Investigator or the study eligibility committee, the patient's life expectancy \< 12 months

Interventions

DEVICE

Trillium™

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Conditions

Tricuspid RegurgitationTricuspid Regurgitation Functional

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