A clinical study to compare among three types of nerve blocks to decrease pain during and after surgeries of penis in childre
Phase 4
- Conditions
- Health Condition 1: Q648- Other specified congenital malformations of urinary systemHealth Condition 2: N488- Other specified disorders of penisHealth Condition 3: N368- Other specified disorders of urethraHealth Condition 4: N364- Urethral functional and muscular disorders
- Registration Number
- CTRI/2024/03/064341
- 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
1-7 years of age
ASA I-II
Undergoing elective surgery
Exclusion Criteria
Patients with known allergies to the study drug
Coagulopathy
Patients with neurological disorders
Patients with spinal deformities
Emergency surgeries
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate postoperative pain scores during 24 hours at different time points (0h, 2h, <br/ ><br>4h, 6h, 12h, 24h) using FLACC pain scale (Face, Leg, Activity, Cry and Consolability) <br/ ><br>delivering postoperative analgesia. <br/ ><br>Timepoint: 0h, 2h, 4h, 6h, 12h, 24h <br/ ><br>
- Secondary Outcome Measures
Name Time Method Time to first rescue analgesiaTimepoint: within 24 hours;To assess parent’s satisfaction with perioperative analgesiaTimepoint: after 24 hours;To assess perioperative opioid consumption among the three groups during 24 hoursTimepoint: within 24 hours