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A study to evaluate Ultrasound guided novel sacral erector spinae block for postoperative analgesia in pediatric patients undergoing hypospadias repair.

A randomized controlled study of Ultrasound guided novel sacral erector spinae block for postoperative analgesia in pediatric patients undergoing hypospadias repair at SMS Medical College, Jaipur. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/089957
Enrollment
66
Registered
2025-07-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: Q64- Other congenital malformations ofurinary system

Interventions

Intervention1: Ultrasound guided novel sacral erector spinae block: Injection of 1ml/kg of 0.25% Bupivacaine Intervention2: Nil: Nil Intervention3: Ultrasound guided novel sacral erector spinae block:

Sponsors

Sawai Man Singh Medical College and attached hospitals, Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for elective hypospadias repair surgery. 2. Guardian willing to give informed written consent. 3. Patient of male sex with age group more than 2 years. 4.American Society of Anesthesiologists (ASA) physical status I-II.

Exclusion criteria

Exclusion criteria: 1. Patient should not be part of any other study. 2. Patient allergic to any drug given during procedure. 3. Patient with local site infection.

Design outcomes

Primary

MeasureTime frame
To assess postoperative analgesic (Paracetamol) consumption (in mgs) over 24 hours.Timepoint: 0,15,30 and 45 minutes, then 1,1.5,2,4,6,8,10,12,18 and 24 hours.—

Secondary

MeasureTime frame
1.To assess time to first rescue analgesic.Timepoint: ;2.To assess postoperative pain using FLACC score.Timepoint: 0,15,30 and 45 minutes, then 1,1.5,2,4,6,8,10,12,18 and 24 hours.;3. To assess side effects associated with block.Timepoint: 0,15,30 and 45 minutes, then 1,1.5,2,4,6,8,10,12,18 and 24 hours.—

Countries

India

Contacts

Public ContactDr Parul Sharma

SMS Medical College

vkothari66@gmail.com982820186

Outcome results

None listed

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