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A clinical study to compare among three types of nerve blocks to decrease pain during and after surgeries of penis in children

Comparison among Ultrasound guided Pudendal Nerve Block Dorsal Penile Nerve Block and Caudal Block for perioperative analgesia on pediatric patients undergoing penile surgeries - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064341
Enrollment
114
Registered
2024-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: Q648- Other specified congenital malformations of urinary system Health Condition 2: N488- Other specified disorders of penis Health Condition 3: N368- Other specified disorders of urethra Health Condition 4: N364- Urethral functional and muscular disorders

Interventions

Intervention1: Pudendal nerve block: Block will be performed in lithotomy position and needle will be inserted under ultrasound guided technique from inferomedial aspect of bilateral ischial tubero

Sponsors

All India Institute Of Medical Sciences Patna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1-7 years of age ASA I-II Undergoing elective surgery

Exclusion criteria

Exclusion criteria: Patients with known allergies to the study drug Coagulopathy Patients with neurological disorders Patients with spinal deformities Emergency surgeries

Design outcomes

Primary

MeasureTime frame
To evaluate postoperative pain scores during 24 hours at different time points (0h, 2h, 4h, 6h, 12h, 24h) using FLACC pain scale (Face, Leg, Activity, Cry and Consolability) delivering postoperative analgesia. Timepoint: 0h, 2h, 4h, 6h, 12h, 24h

Secondary

MeasureTime frame
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

Countries

India

Contacts

Public ContactDr Shagufta Naaz

AIIMS Patna

drshaguftanaaz@gmail.com7765937919

Outcome results

None listed

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