Coronary Heart Disease Complicated With Ischemic Mitral Regurgitation in China

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChina National Center for Cardiovascular Diseases

About this trial

This project will rely on the established multi-center cooperation platform for total valve disease and based on the Carpentier classification, which is newly proposed and widely recognized by the academic community, and will specifically target the population with coronary heart disease combined with Ischemic Mitral Regurgitation(IMR) to conduct a nationwide, multi-center, single valve disease, prospective cohort. Research. From November 2025 to December 2025, 6,000 patients with coronary heart disease combined with moderate or above IMR were consecutively selected from outpatients or inpatients in 21 regional medical centers across the country, and clinical characteristics, imaging data, and serology were collected. Information, drug/surgical intervention status and clinical outcome indicators were included in the clinical follow-up at baseline, 3 months, 6 months, 12 months and 24 months respectively. The main research objectives are to describe the disease characteristics, treatment status and clinical outcomes of coronary heart disease patients with IMR; to evaluate the current application status of GDMT strategies in IMR diagnosis and treatment practice and its impact on mid- and long-term prognosis. The secondary research objectives are to identify factors affecting prognosis, construct a risk stratification model for mid- and long-term prognosis, and discover new molecular markers.

This project will for the first time construct the world's largest clearly defined cohort of coronary heart disease combined with IMR. Its research results can provide high-quality data and decision-making basis for precise diagnosis and treatment of IMR populations. Therefore, this project has important scientific research value and clinical guidance significance.

Eligibility criteria

Qualifiers

Age ≥18 years, secondary mitral regurgitation discovered during outpatient visit or hospitalization;

Have definite coronary heart disease

Segmental wall motion abnormality or

Mitral regurgitation is consistent with Carpentier type IIIb (eccentric regurgitation)

Disqualifiers

Patients within the past year or currently participating in other clinical studies;

Primary mitral regurgitation (such as mitral valve prolapse, perforation, chordae tendineae rupture, etc.);

Dilated cardiomyopathy, hypertrophic cardiomyopathy and other diseases;

Moderate and above aortic stenosis/regurgitation, mitral stenosis, tricuspid stenosis, etc.;

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

6,000 Participants
are grouped into 2 trial groups

Locations

This trial has no locations