Comparison of two pain relief methods for liver donation surgery
Phase 3
- Conditions
- Health Condition 1: K769- Liver disease, unspecified
- Registration Number
- CTRI/2024/05/067658
- Lead Sponsor
- Dr Rachana C Nair
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All adult patients aged 18 - 60 years, undergoing open live donor hepatectomy
Exclusion Criteria
Patient refusal
Contraindication to neuraxial anesthesia
Allergy to local anesthetics
Insufficient comprehension to use of IVPCA
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare postoperative fentanyl consumption at 48 hours between the two groups.Timepoint: To compare postoperative fentanyl consumption at 48 hours between the two groups.
- Secondary Outcome Measures
Name Time Method To compare the intraoperative IV fentanyl requirements in both groups <br/ ><br>To compare the time of first rescue analgesia requirement in both the groups <br/ ><br>To compare the postoperative pain using NRS in both the groups <br/ ><br>To compare the intraoperative fluid requirements in both the groups <br/ ><br>To compare the rate of complications in both the groupsTimepoint: Baseline, intraoperative at 15 minutes interval, postoperative till 48 hours