Abbott Cephea Mitral Valve Disease Registry

This is a registry, which means it collects information about patients with mitral valve disease, including mitral regurgitation (a leaky heart valve), mitral stenosis (a narrowed heart valve), and mixed mitral valve disease. The goal is to better understand how treating these conditions affects patients, especially those who might receive a new treatment called Transcatheter Mitral Valve Replacement (TMVR) using the Cephea Mitral Valve System. You might be able to join if you are 18 or older, have symptomatic mitral valve disease, and your heart team believes TMVR is a good option for you. The study aims to gather data for up to two years after you enroll.

Study design
This is an observational study that plans to enroll 1000 participants. It is not testing a specific intervention but rather collecting information about patients.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed from enrollment up to 2 years.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07069673

Abbott Cephea Mitral Valve Disease Registry

Recruiting
Not specifiedAges 18+Observational
Abbott Medical Devices
~1,000 participants
Updated 2026-06-22 on ClinicalTrials.gov

At a glance

Recruiting sites
23 of 23 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Primary Objective
Measured over From enrollment to 2 years of follow-up
Mitral Regurgitation
Mitral Stenosis
Mitral Valve Disease
Mitral Valve (MV) Regurgitation
Mitral Annulus Calcification
Mitral Valve Replacement
Transcatheter Valve Replacement
23 sites across 18 states
Tennessee3
Georgia2
New York2
Texas2
Alabama1
Arizona1
California1
Illinois1

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  • Primary ObjectiveFrom enrollment to 2 years of follow-up

    The objective of the MVD Registry is to collect data on the progression of MVD patients considered for TMVR therapy to guide product development, regulatory submissions, and reimbursement planning