A study conducted to evaluate pain relief by nerve block in patients undergoing robotic assisted and minimally invasive cardiac surgeries.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/05/067613
- Lead Sponsor
- Dr Amit Rastogi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anaesthesiologists physical status II and III with New York Heart
Association grading I and II, scheduled for Robotic assisted and minimally invasive direct
coronary artery bypass Surgeries under general anaesthesia.
Exclusion Criteria
Patients with uncontrolled medical diseases, psychiatric ailments, coagulopathy, infection at
the local site, chronic opioid usage, obstructive sleep apnoea and patient refusal.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Static and Dynamic pain assessment using mean VAS scoreTimepoint: After arrival in the ICU (0 hour), then at 6-hourly intervals for a period of 48 hours
- Secondary Outcome Measures
Name Time Method Mean opioid consumption, measurement of peak expiratory <br/ ><br>flow rate 24 hours and 48 hours post extubation, assessment of postoperative nausea and <br/ ><br>vomiting (PONV), requirement of rescue antiemetic, pruritus and respiratory depression.Timepoint: After arrival in the ICU (0 hour), then at 6-hourly intervals for a period of 48 hours