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To evaluate the myocardial viability of the mitral papillary muscle-ventricular wall complex to guide the surgical treatment of moderate ischemic mitral insufficiency

To evaluate the myocardial viability of the mitral papillary muscle-ventricular wall complex to guide the surgical treatment of moderate ischemic mitral insufficiency

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042454
Enrollment
Unknown
Registered
2021-01-21
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic mitral insufficiency

Interventions

control group:coronary artery bypass grafting
experimental group:coronary artery bypass grafting +MVP

Sponsors

Beijing Institute of Heart Lung and Blood Vessel Disease
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients who have symptoms and confirmed coronary artery disease with left main artery disease, three-vessel disease, and proximal anterior descending artery disease who are scheduled to undergo coronary artery bypass grafting; (2) Echocardiographic diagnosis of moderate mitral valve Criteria for insufficiency: it can be diagnosed if any two of the following criteria are met (effective mitral regurgitation orifice area: 0.2-0.4 cm2, regurgitant beam width: 3-7mm, mitral regurgitation area and left atrium area The ratio is 20%-40%); (3) Aged 18-75 years.

Exclusion criteria

Exclusion criteria: (1) Mitral valve structure disease (valve leaf calcification, adhesion, perforation, prolapse, mucoid change, annulus calcification, subvalvular structure calcification, adhesion, contracture, lengthy); (2) Transthoracic echocardiography is not available Effective regurgitation orifice and left ventricular end-systolic volume index; (3) Combined with other cardiac operations; (4) Past mitral valve surgery history; (5) Cardiopulmonary bypass contraindications; (6) Cardiogenic shock at the time of admission (7) Two weeks before the patients admission, the patient has long-term intravenous use of inotropic drugs; (8) The patient has ST-segment elevation myocardial infarction that requires intervention within 7 days before admission; (9) With advanced malignant tumors, The expected survival time is less than 1 year.

Design outcomes

Primary

MeasureTime frame
Resting myocardial perfusion imaging;Myocardial survival of mitral valve papillary muscle-ventricular wall complex;Left ventricular end systolic volume index;

Secondary

MeasureTime frame
All cause death;Stroke;Reoperation of mitral valve;Readmission for heart failure;NYHA cardiac function increased by 1-2 grades;Increased mitral regurgitation;Other serious adverse events;

Countries

China

Contacts

Public ContactYongqiang Lai

Beijing Institute of Heart Lung and Blood Vessel Disease

yongqianglai@yahoo.com+86 10-64456776

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026