To study the improvement of ischemic moderate mitral regurgitation after coronary artery bypass grafting only and not mitral valve replacement.
Not Applicable
- Conditions
- Health Condition 1: I340- Nonrheumatic mitral (valve) insufficiency
- Registration Number
- CTRI/2022/05/042900
- Lead Sponsor
- fortis escorts heart institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with moderate mitral regurgitation and coronary artery disease undergoing elective coronary artery bypass grafting.
Patients with informed written consent.
Exclusion Criteria
Patients with mitral regurgitation due to rheumatic, infectious, degenerative, congenital, papillary muscles rupture, elongated chordae tendineae.
Patients not giving informed consent.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method