EVOQUE System for Heart Valve Replacement

Real World European Investigation of Safety and Clinical Efficacy of the EVOQUE System (TRISCEND III EU)

Recruiting Observational Study
Tricuspid Valve Regurgitation Heart Valve Diseases Cardiovascular Diseases
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Sex
Any
Study type
Observational
Participants needed
500 (estimated)
Sponsor
Edwards Lifesciences · Industry
Who this trial is looking for

This trial is looking for patients who need a special heart procedure called transcatheter tricuspid valve replacement. Participants will receive the EVOQUE system and will need to attend follow-up appointments to see how they are doing.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am suitable for the EVOQUE system treatment as decided by the heart team.
  • I agree to attend follow-up assessments.
  • I have given written consent to take part in this study.

You may not be able to join if

  • I am currently in another clinical study for a treatment.
  • I am considered part of a vulnerable population.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial

This is a prospective, single-arm, multi-center, real-world study of an the Edwards EVOQUE system.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. The Local Site Heart Team determines that the patient is appropriate for transcatheter tricuspid valve replacement with the EVOQUE system per the current instructions for use. 2. Patient agrees to attend follow-up assessments. 3. Patients provided written informed consent for…
Contacts

TMTT Clinical

+1-949-250-2500 or

TMTT_Clinical@Edwards.com

CONTACT