Ischemic Mitral Regurgitation

4

Review clinical trials related to Ischemic Mitral Regurgitation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Coronary Heart Disease Complicated With Ischemic Mitral Regurgitation in China

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.

Participants needed: 6,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: China National Center for Cardiovascular DiseasesUpdated: Nov 17, 2025Duration: 2 Years
Eligibility criteria

Age ≥18 years, secondary mitral regurgitation discovered during outpatient visit... [+4]

Patients within the past year or currently participating in other clinical studi... [+4]

Status: Recruiting

Treatment of Moderate Ischemic Mitral Regurgitation in Patients With Coronary Artery Disease

This study aims to evaluate the effect of angiotensin receptor/neprilysin inhibitors (ARNI) on improving ischemic mitral regurgitation (IMR) in patients with coronary artery disease undergoing isolated coronary artery bypass grafting (CABG) through a randomized controlled clincial trial.

Participants needed: 220
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: China National Center for Cardiovascular DiseasesUpdated: Aug 27, 2025Locations: 1
Eligibility criteria

Fully informed and voluntarily signed informed consent; [+1]

Status: Recruiting

Serotonin Receptor Blockers in Ischemic Mitral Regurgitation

This study is intended to investigate the effect of cyproheptadine (a 5HT2B receptor blocker) on mitral regurgitation severity.

Participants needed: 214
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: Laval UniversityUpdated: Nov 15, 2023Locations: 1
Eligibility criteria

Patients 18-80 years old with a 1st episode of STEMI with documented coronary ob... [+1]

Inability to provide informed consent [+13]

Status: Not yet recruiting

Epicardial Mitral Touch System for Mitral Insufficiency

To evaluate the safety and performance of the Mitral Touch System to treat mitral insufficiency in patients who are to undergo cardiac surgery with either a sternotomy or thoracotomy who present with moderate to severe ischemic or functional mitral regurgitation.

Participants needed: 10
Trial details
Age: 22+Biological sex: AllType: InterventionalSponsor: Mitre Medical Corp.Updated: Jan 4, 2023Locations: 1
Eligibility criteria

Moderate or greater (2+) ischemic [+5]

Any evidence of structural (chordal or leaflet) mitral valve disease [+20]