Assessment of Postoperative Analgesia in Bypass Surgeries with different Blocks
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/07/035045
- Lead Sponsor
- prathima institute of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients who have been planned for elective coronary artery by-pass graft (CABG) under general anaesthesia to address triple vascular disease
Exclusion Criteria
hemodynamic instability, signs of congestive heart failure, preexisting infection at the block site, allergy to local anaesthetics, mental disease, and a protracted postoperative ventilatory course
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method postoperative pain with visual analog scaleTimepoint: 0,3,6,12,24 hours post extubation
- Secondary Outcome Measures
Name Time Method need for fentanyl infusionTimepoint: first 24 hours postoperative