ClinicalTrials.Veeva

Menu

European Registry of Transcatheter Repair for Tricuspid Regurgitation (EuroTR)

L

LMU Klinikum

Status

Enrolling

Conditions

Valvular Heart Disease
Heart Failure
Tricuspid Regurgitation

Treatments

Device: T-TEER

Study type

Observational

Funder types

Other

Identifiers

NCT06307262
EuroTR Registry

Details and patient eligibility

About

To investigate clinical and survival outcomes following transcatheter tricuspid valve repair or replacement.

Full description

Background and Rationale:

Tricuspid regurgitation (TR) is a major health and economic burden due to high rates of heart failure hospitalizations, morbidity and mortality. Surcial treatment of TR is associated with high procedural and in-hospital mortality. Due to prohibitive surgical risk, a significant proportion of patients historically remained untreted beyond medical therapy. Transcatheter tricuspid valve (TV) repair and replacement techniques (TTVT) now offer a new treatment perspective for these patients. The EuroTR registry aims at optimizing patient selection prior to TTVT and thus treatment quality by collecting respective data in a real-world setting.

Objectives:

To investigate clinical and survival outcome following transcatheter tricuspid valve repair or replacement.

Enrollment

3,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients treated with one of the following transcatheter devices for TV repair or replacement: PASCAL, TriClip, TricValve, Evoque, LuX-Valve
  • Age ≥ 18 years

Trial contacts and locations

1

Loading...

Central trial contact

Jörg Hausleiter, Prof. Dr.; Lukas Stolz, Dr.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems