🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Germany / NCT06212193
Recruiting Not applicable

Innoventric Trillium™ Stent Graft Early Feasibility Study (EFS)

NCT06212193 · tracked via the Priya Life Science Germany tracker
Sponsor
Innoventric LTD
Phase
Not applicable
Started
2024-08-05
Last updated
2025-03-07

Condition(s) studied

Tricuspid RegurgitationTricuspid Regurgitation Functional

Investigational drug(s) / intervention(s)

Trillium™

Trillium™: Trillium™ Stent Graft for Cross-Caval Tricuspid Valve Replacement

Study 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).

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (12)

FacilityCityRegionStatus
Cardiovascular Institute of Los Robles Health System Thousand Oaks California Recruiting
Ascension St. John Detroit Michigan Recruiting
Mayo Clinic Hospital (Rochester) Rochester Minnesota Recruiting
Weill Cornell Medicine New York New York Recruiting
Stony Brook Heart Institute Stony Brook New York Recruiting
The Christ Hospital Cincinnati Ohio Recruiting
Lankenau Heart Institute Philadelphia Pennsylvania Recruiting
TriStar Centennial Medical Center Nashville Tennessee Recruiting
University of Washington Medical Center Seattle Washington Recruiting
University Medicine Mainz Mainz Rhineland-Palatinate Recruiting
Helios Health Institute GmbH, Leipzig Leipzig Saxony Recruiting
German Heart Center at Charité (DHZC) Berlin State of Berlin Recruiting

More Innoventric LTD trials in Germany

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06212193 on ClinicalTrials.gov ↗ ← All trials in Germany