Comparison of peripheral regional blocks with ultrasonography for post operative pain relief in laparoscopic cholecystectomy patients
Phase 3
Completed
- Registration Number
- CTRI/2020/10/028603
- Lead Sponsor
- Dr Asha Devanand
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
patients undergoing laparoscopic cholecystectomy
Exclusion Criteria
patient refusal, ASA III-IV, contraindication to regional anaesthesia, bleeding diathesis
use of anticoagulants, hypertension, known allergy to local anaesthetics, advanced hepatic or renal failure, advanced psychiatric illness, obesity- bmi >35kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method analgesic efficacy to be measured by numeric rating scaleTimepoint: at the end of surgery as block given to 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method total rescue analgesic consumption in 24 hours, hemodynamic parameters and any complicationsTimepoint: postoperative 20 minutes after giving block to 24 hours follow up