Minimally invasive versus conventional surgical aortic valve replacement: retrospective multicentre-study
Recruiting
- Conditions
- Aortic (valve) stenosisI35.0
- Registration Number
- DRKS00025211
- Lead Sponsor
- Robert-Bosch-Krankenhaus
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 5000
Inclusion Criteria
Adult men and women (>= 18 years)
-Indication for surgery: aortic valve vitium
-Possibly additional procedures: supracommissural replacement of ascending aorta, atrial ablation, resection of left atrial appendage, subvalvular resection (Morrows operation).
-Informed consent to study participation (given during follow up visitation)
Exclusion Criteria
-Emergency operation
-Re-operation
-Endocarditis
-Combined surgery other than above-mentioned
-Denial or inability of consent to study participation
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method MACCE (death, myocardial infarction, stroke, reoperation) after 30 days an in follow-up (up to 5 years); questionnaire and telephone interview
- Secondary Outcome Measures
Name Time Method blood transfusion, conversion to sternotomy, sternal wound healing disorder/ infection, postpericardiotomy syndrome, length of hospital stay, rehospitalisation