To study a pain relief technique in patients undergoing cardiac surgeries
Phase 4
- Conditions
- Health Condition 1: null- Patients undergoing elective cardiac surgeries under median sternotomy
- Registration Number
- CTRI/2018/05/013578
- Lead Sponsor
- Department of Anesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 2-3 Patients undergoing elective cardiac surgeries through median sternotomy
Exclusion Criteria
Emergency or redo sternotomy cardiac surgeries, difficult to wean from Cardiopulmonary bypass, requiring more than two inotropic support to wean from CPB, requiring prolonged postoperative ventilation, suspecting bleeding disorders or coagulopathy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method