A clinical trial to compare the efficacy of two plane blocks,ultrasound-guided erector spinae plane block and ultrasound-guided transversus abdominis plane block for post-operative analgesia in children undergoing lower abdominal surgery under general anaesthesia.
Not Applicable
- Conditions
- Health Condition 1: G891- Acute pain, not elsewhere classified
- Registration Number
- CTRI/2023/07/054892
- Lead Sponsor
- Department of Anaesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age 6 months to 7 years.
2. ASA grade I
3. Patients undergoing lower abdominal surgery.
Exclusion Criteria
1.Refusal of Consent from parents.
2. Allergy to local anaesthesia
3.Infection at injection site
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Average CHEOPS score till first rescue analgesia.Timepoint: After the arrival of the patient in the recovery room at 15 minutes, 30 minutes, 1, 2, 4, 6, 9 & 12 hours.
- Secondary Outcome Measures
Name Time Method 1. Total rescue analgesia given in 12 hours. <br/ ><br>2. Time taken for the first rescue analgesia.Timepoint: 1. First 12 hours of postoperative period <br/ ><br>2.No specific time points.