comparing analgesic efficacy of two different drugs when given in caudal blocks in pediatric patients undergoing sub umbilical surgeries
Not Applicable
- Conditions
- Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangreneHealth Condition 2: N472- ParaphimosisHealth Condition 3: N471- Phimosis
- Registration Number
- CTRI/2023/10/058793
- Lead Sponsor
- Mahatma Gandhi Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American society of Anaesthesiologists (ASA) physical status I/II patients.
Patients aged between 1-10 yr.
Patients with both male and female gender.
Duration of surgery less than 2 hrs.
Patients posted for surgery in subumbilical region.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time required for first rescue analgesiaTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Hemodynamic stability & sensory motor blockTimepoint: 3hours