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CHoice of OptImal transCatheter trEatment for Mitral Insufficiency Registry

RecruitingObservational study

Choice of Optimal Transcatheter Treatment for Mitral Insufficiency Registry

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* clinically significant mitral insufficiency
* patient underwent screening for TMVI
* echocardiography data at baseline (and after TMVI, E2E and surgery)
* follow-up of at least 30 days

Exclusion Criteria:

\- age under 18 years

About the study

This multinational, investigator-initiated registry aims to investigate clinical outcomes of patients undergoing transcatheter mitral valve replacement (TMVR). The registry primarily focuses on patients treated with TMVR in real-world clinical practice.

Patients evaluated for TMVR but not undergoing the procedure are no longer systematically included. Historical data may include such patients who subsequently underwent alternative treatments, including transcatheter edge-to-edge repair, mitral valve surgery, or medical/conservative therapy.

Sponsor: Universitätsklinikum Hamburg-Eppendorf · Participants: 1,000 · Started: Nov 1, 2020

Contact the study team

Official record on ClinicalTrials.gov — NCT04688190

Locations in the U.S.

ArizonaTucson Medical Center, Tucson
CaliforniaCedars-Sinai Medical Center, Los Angeles, Los Angeles
FloridaTampa General Hospital, Tampa
MassachusettsBrigham and Women's Hospital, Boston
MinnesotaMinneapolis Heart Institute at Abbott Northwestern Hospital, Minneapolis
New JerseyMorristown Medical Center, Morristown
New YorkMontefiore Medical Center, New York
OklahomaOklahoma Heart Hospital, Oklahoma City
TexasHouston Methodist Hospital, Houston

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.