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Clinical Trials in Germany / NCT05825898
Enrolling by invitation Observational

Outcome of Patients With Severe Functional TR According to Medical, Transcatheter or Surgical Treatment

NCT05825898 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2022-09-01
Last updated
2026-05-08

Condition(s) studied

Tricuspid Regurgitation

Investigational drug(s) / intervention(s)

Surgery or Transcatheter tricuspid valve intervention

Surgery or Transcatheter tricuspid valve intervention: Isolated tricuspid valve surgery or Transcatheter tricuspid valve intervention

Study summary

Tricuspid regurgitation (TR) is a public health problem: moderate / severe TR are common, especially in ageing populations, and affect 4% of the population \>75 years old, totaling approximately 1.6 million in the US and 3 million in Europe. TR is associated with an increased risk of mortality and morbidity. Contrasting with TR prevalence and the magnitude of the problem, the vast majority of patients are medically treated with diuretics to relieve their symptoms and a curative surgical treatment for isolated severe TR is seldom performed. Reluctance to perform an ITVS can be explained in the one hand by the limited evidence that TR correction improves outcomes and on the other hand, ITVS is associated to high observed in-hospital mortality rates (≈ 10% remarkably consistent in most series across the literature). Severity of the clinical presentation is the main predictor of outcome after surgery. The TRI-SCORE, is a dedicated, simple and accurate risk score model to predict in-hospital mortality after ITVS that could guide the clinical decision-making process at the individual level. Excellent outcomes can be achieved when patients present with low TRI-SCORE. These results suggest adopting a more pro-active approach for TV interventions, and to intervene earlier in the course of the disease in patients with severe isolated TR, irrespective of TR mechanism / etiology, before the occurrence of advanced / irreversible consequences such as severe RV dilatation / dysfunction, renal and liver failure, and intractable heart failure. Recently transcatheter tricuspid valve interventions (TTVI) have emerged recently as a less invasive option to surgery to cure patients with TR.

What is the best treatment between medical, surgical or transcatheter therapy to consider and the best timing for each patient are not clearly defined. The aim of the study is to compare outcome of patients with significant functional TR according to medical, transcatheter or surgical treatment after matching per TRISCORE.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Isolated (no left-valvular heart disease (mitral regurgitation) \>2) * AND Functional * AND Moderate to severe or severe Tricuspid regurgitation Exclusion Criteria: * Congenital valvular disease, * Previous tricuspid valve intervention, * Organic tricuspid valvular disease * Associated valvular heart disease

Primary outcome measure(s)

Trial sites (44)

FacilityCityRegionStatus
Mayo Clinic Rochester Rochester Minnesota
Mount Sinai New York New York
Columbia University Medical Center New York New York
Montefiore Health System New York New York
Vienna Medical University Vienna Austria
University of Ottawa Heart Institute Ottawa Ontario
IUCPQ Québec Canada
St Michael's Hospital Toronto Canada
St Paul Hospital Vancouver Canada
Amiens University Hospital Amiens France
Henri Mondor Hospital Créteil France
CHU Lille Lille France
Department of Cardiovascular Surgery and Transplantation, Louis Pradel Cardiovascular Hospital Lyon France
APHM, La Timone Hospital, Cardiology Department Marseille France
Department of Cardiology, University Hospital of Nancy-Brabois Nancy France
CHU de Nantes Nantes France
Department of Cardiology, Bichat Claude Bernard Hospital Paris France
CHU de RENNES Rennes France
CHU Charles Nicolle Rouen France
Cardiology Department, Centre Cardiologique du Nord Saint-Denis France
Rangueil University Hospital Toulouse France
Herz- und Diabeteszentrum Bad Oeynhausen Germany
Charité Universitätsmedizin Berlin Berlin Germany
Bonn University Hospital Bonn Germany
University of Cologne Cologne Germany
Cardiovascular center Frankfurt Frankfurt Germany
Albertinen Heart and Vascular Center Hamburg Germany
Asklepios clinic Sankt Georg Hamburg Germany
University Heart and Vascular Center Hamburg Germany
Leipzig University Hospital Leipzig Germany
University Medical Center of Mainz Mainz Germany
Munich Großhadern Munich Germany
Tel Aviv Medical center Tel Aviv Israel
Instituto Auxologico Italiano, IRCCS Milan Italy
San Raffaele University Hospital Milan Italy
Leiden University Medical center Leiden Netherlands
Hospital 12 de Octubre Madrid Spain
Hospital Clínico San Carlos Madrid Spain
Hospital Gregorio Marañón Madrid Spain
Hospital Ramón y Cajal Madrid Spain

+ 4 more sites — see the full list on the official registry below.

More Ottawa Heart Institute Research Corporation 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 NCT05825898 on ClinicalTrials.gov ↗ ← All trials in Germany