A clinical trial to compare the effect of drug ropivacaine when given via two routes, erector spinae plane block and peritubal local infiltration for post operative pain management in patients undergoing percutaneous nephrolithotomy surgery.
Phase 4
- Conditions
- Health Condition 1: N200- Calculus of kidneyHealth Condition 2: N00-N99- Diseases of the genitourinary system
- Registration Number
- CTRI/2023/08/056925
- Lead Sponsor
- Mahatma Gandhi Medical College And Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age (18-65) years
2.All genders
3.Patients with ASA grade I/II
4.Patients undergoing PCNL surgery under GA
Exclusion Criteria
1.Infection at local site
2.H/o drug abuse, psychiatric disorder, chronic pain
3.Coagulation abnormalities
4.Pregnant or lactating females
5.Refusal for consent of peripheral nerve block
6.History of drug allergy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the post operative pain score of two groups (Erector Spinae Plane Block & Peritubal infiltration of LA) using Visual Analogue Scale (VAS)Timepoint: Post-operative pain score monitoring by VAS score at 30min, 60min, 2h, 4h, 8h, 12h, 16h, 20h & 24hour.
- Secondary Outcome Measures
Name Time Method 1) To compare time to first rescue analgesia in both groups. <br/ ><br>2) To compare total consumption of analgesics in first 24 hours post operatively. <br/ ><br>3) To compare patient satisfaction in both groups. <br/ ><br>4) Comparison of occurrence of any complication in either group.Timepoint: first 24 hours post operatively