Evaluation and comparison between 0.125% vs 0.25% bupivacaine for ultrasound guided sacral erector spinae block in paediatric patients undergoing hypospadias repair.

Comparison of 0.125% vs 0.25% bupivacaine for ultrasound guided sacral erector spinae block in paediatric patients undergoing hypospadias repair .

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/03/050226

Enrollment

Registered

2023-03-02

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Q549- Hypospadias, unspecified Health Condition 2: N488- Other specified disorders of penis Health Condition 3: N488- Other specified disorders of penis

Interventions

Intervention1: ultrasound guided sacral erector spinae block using 0.25% Bupivacaine in paediatric patients undergoing hypospadias repair: Ultrasound guided sacral erector spinae plane block in paedia

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
Time for requirement of first rescue analgesic Timepoint: Pain assessment will be done postoperatively using VAS score at 0 hr, every 15 mins upto 1 hr, every half an hour upto 2 hours, 2 hrly upto 12 hours and then at 18th hour and 24 th hour postoperatively.	—

Secondary

Measure	Time frame
1) Total intraoperative fentanyl consumption 2) Post-operative pain score 3) Post-operative analgesic consumption in 24hrs 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.	—

Measure

Time frame

1) Total intraoperative fentanyl consumption 2) Post-operative pain score 3) Post-operative analgesic consumption in 24hrs 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.

—

Countries

India

Contacts

Public ContactDr Bharti Singla

Pt. B.D. Sharma PGIMS ROHTAK

drbhartibs@gmail.com9009369698

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026