Study of two block in laproscopic pyeloplasty for post operative pain relief
Not Applicable
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2022/12/048155
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of either sex aged 18-65 years
ASA grade I-II patients scheduled to undergo elective laparscopic pyeloplasty under GA
Exclusion Criteria
Patients not giving consent
Local infection at site of block
H/o allergy to study medications
Patients taking α agonist / antagonist regular pain medication
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time for first rescue analgesic requirementTimepoint: After end of surgery at: 0 minutes, 30 minutes, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours
- Secondary Outcome Measures
Name Time Method Visual Analogue scale for pain (ranging from 0 to 10, where 0 no pain and 10 maximum pain) will be evaluated postoperatively at 30 min and 2, 4, 6, 12, and 24 h postoperative <br/ ><br>Timepoint: 24hrs