A clinical trial to compare the effectiveness of three regional blocks for post-operative pain in children undergoing inguinal hernia repair
Phase 3
Completed
- Conditions
- Health Condition 1: N40-N53- Diseases of male genital organs
- Registration Number
- CTRI/2019/09/021377
- Lead Sponsor
- All India Institute of Medical SciencesBhubaneswar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I and II functional status
Exclusion Criteria
refusal to give consent
known allergy to local anesthetics
coagulopathy
infection at the injection site
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time for the first demand of rescue analgesia in minutesTimepoint: Time for the first demand of rescue analgesia in minutes
- Secondary Outcome Measures
Name Time Method 1. Comparison of post operative FLACC scores.Timepoint: post operative 24 hrs;2.Total cumulative Paracetamol and Fentanyl requirement in post operative periodTimepoint: post operative till discharge from hospital;3. Comparison of intraoperative Fentanyl requirement among the three groupsTimepoint: Intraoperative;4. Total duration for performance of blockTimepoint: intraoperative