A clinical trial to study efficiency of two blocks, erector spinae plane block and transversus abdomisis plane block for post operative pain relief in elective laproscopic abdominal surgeries
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/09/057222
- Lead Sponsor
- Dr Ajay Kamboj
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Asa I and II
2. Patient undergoing elective laproscopic surgery under General Anesthesia
3. Patient willing to participate in study after due consent
Exclusion Criteria
1. Patient with significant cardiopulmonary disease
2.Patient with Neurological and psychiatric disease
3.Patient with allergy to medicine used in study
4. Contraindications to regional Anesthesia
5. Patient with spinal deformity
6.Patient unwilling to participate in study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Erector spinae plane block provide better pain relief than transverse abdominis plane block for post operative pain in elective laproscopic abdominal surgeryTimepoint: Assess Numerical rating score for analgesia evaluation at one hour,six hour,12 hour,18 hour , 24 hour
- Secondary Outcome Measures
Name Time Method 1.Total post operative opioid consumption <br/ ><br>2. Time for breakthrough pain.Timepoint: Total opioid consumption in 24 hour