Ropivacaine heavy 0.75% vs Bupivacaine heavy 0.5% in infraumbilical surgeries for duration of analgesia
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064555
- Lead Sponsor
- Jawahar lal nehru medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Body weight 40 to 80 kg
2. ASA class I and II
3. patients undergoing infraumblical surgeries
Exclusion Criteria
1.Patients refusal and uncooperative patients
2.Hypersensitivity to study drugs
3. local site infection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method duration of analgesiaTimepoint: pain will be assessed using Visual Analogue Score in immediate postoperative period follwoed by hourly interval till 24 hrs post opertively
- Secondary Outcome Measures
Name Time Method 1. onset and duration of sensory block <br/ ><br>2.onset and duration of motor block <br/ ><br>3. hemodynamic changes and adverse effectsTimepoint: 1.using hypodermic needle immediately after spinal, every 2 minutes till 10minut, every 5minute till 60minute then every hour till 6 hour in post operative period then every 6hour till 24 hour. <br/ ><br> <br/ ><br>2.Assessed using Bromage score immediately after spinal, every 2 minutes till 10minut, every 5minute till 60minute then every hour till 6 hour in post operative period then every 6hour till 24 hour.