A clinical trial to assess the effect of nerve block in children undergoing lower abdominal surgeries
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056159
- Lead Sponsor
- All India Institute of Medical Sciences, Patna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I and II patients scheduled for upper abdominal surgeries with unilateral incisions
Exclusion Criteria
Parent refusal to participate in the study
Patients hypersensitive to study medications
Patients with developmental or mental delay
Skin lesions or infection at the planned site of needle insertion
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total Intraoperative fentanyl consumption <br/ ><br> <br/ ><br>Timepoint: 5, 30, 60, and 90 minutes after skin incision and at the end of surgery <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method Postoperative pain score using FLACC score at 1, 4, 8, 16, 24 hours at rest. <br/ ><br>To determine time to first rescue analgesic administration <br/ ><br>To estimate total Tramadol consumption 24 hours postoperatively <br/ ><br>Side effect likes nausea, vomiting and sedation and local anaesthetic toxicity <br/ ><br>Timepoint: 1,4,8,16,24 hours