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Taking peopleNo phase

Follows people with severe tricuspid heart valve leakage after TricValve treatment

Follows patients with severe tricuspid regurgitation treated with the TricValve device over time.

Plain-language title generated from the registry record
Registry title: Retrospective Prospective Multicentric Clinical Follow up of Patients After Being Treated With TricValve®

Key facts

Where
Aalst, BelgiumSee the site

Where in Belgium

  • Department of Cardiology, Algemeen Stedelijk Ziekenhuis (ASZ)Aalst, BelgiumNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
P+F Products + Features GmbH
Trial code
NCT05114850
Record updated
3 April 2024
Original description
Retrospective prospective Multicentric clinical follow up of patients with severe tricuspid regurgitation after being treated with the TricValve® Transcatheter Bicaval Valves System.Read full original descriptionShow less

TRICUS REGISTRY - Retrospective Prospective Multicentric Clinical Follow up of Patients With Severe Tricuspid Regurgitation After Being Treated With the TricValve® Transcatheter Bicaval Valves System.

Retrospective prospective Multicentric clinical follow up of patients with severe tricuspid regurgitation after being treated with the TricValve® Transcatheter Bicaval Valves System.

Inclusion: Successful treatment with TricValve Transcatheter Bicaval Valves System; Patient/patient's authorized legal guardian gives his consent to participate in the study and signed the corresponding inform consent.

Exclusion: no exclusion criterion.

ClinicalTrials.gov NCT05114850