Evaluation and comparison between 0.125% vs 0.25% bupivacaine for ultrasound guided sacral erector spinae block in paediatric patients undergoing hypospadias repair.
Phase 3
Completed
- Conditions
- Health Condition 1: Q549- Hypospadias, unspecifiedHealth Condition 2: N488- Other specified disorders of penisHealth Condition 3: N488- Other specified disorders of penis
- Registration Number
- CTRI/2023/03/050226
- Lead Sponsor
- Pt. B.D. Sharma PGIMS Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
Paediatric male patients aged 8 to 12 yrs with American Society of
Anesthesiologists (ASA) physical status I or II scheduled to undergo surgery for hypospadias
repair will be included in the study.
Exclusion Criteria
Patients with
history of developmental delay,
allergic reactions to local anaesthetic
infection at the needle insertion site
bleeding disorders and on anticoagulants
parental refusal shall not be included in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time for requirement of first rescue analgesic <br/ ><br>Timepoint: Pain assessment will be done postoperatively using VAS score at 0 hr, every 15 mins upto 1 <br/ ><br>hr, every half an hour upto 2 hours, 2 hrly upto 12 hours and then at 18th hour and 24 <br/ ><br>th hour <br/ ><br>postoperatively.
- Secondary Outcome Measures
Name Time Method 1) Total intraoperative fentanyl consumption <br/ ><br>2) Post-operative pain score <br/ ><br>3) Post-operative analgesic consumption in 24hrs <br/ ><br>4) Complications, if any[Respiratory depression ,vomiting, others if any, shall be recorded and managed accordingly]Timepoint: Postoperative pain score using the VAS score at 0 hr, every 15 mins upto 1 hour, every half an hour upto 2 hours , 2 hourly upto 12 hours and then at 18th and 24th hour post operatively. <br/ ><br>