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Comparison of two different regional block techniques for analgesic efficacy in pediatric patients undergoing open hip surgeries

Ultrasound-guided caudal epidural Versus PENG Block as a part of the opioid-sparing multimodal analgesic regime for pediatric open hip surgery: A comparative prospective Randomized Clinical Trial - nil

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085756
Enrollment
70
Registered
2025-04-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided PENG Block Group: In Group PENG, the patient will be positioned in a supine position. The anatomical landmarks, including IPE, the iliopsoas muscle and tendon, the fem

Sponsors

Nizams Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) physical status class I II and scheduled for elective unilateral hip surgery due to hip avascular necrosis, dislocation, dysplasia or fracture.

Exclusion criteria

Exclusion criteria: Children diagnosed with neurological, spinal, or coagulation disorders, infections suspected or confirmed to be related to block sites, histories of allergies to local anesthetics (LAs), bilateral or redo hip surgeries, and parents who refused to participate in the study will be excluded

Design outcomes

Primary

MeasureTime frame
to evaluate the postoperative pain scores in the first 24 hours after surgery in patients undergoing hip surgery receiving either PENG or caudal epidural block.Timepoint: intraoperatively after administration of the block and at 30,60,90,120min,6,12 and 24hours postoperatively.

Secondary

MeasureTime frame
time to first request opioid analgesics, total opioid consumption in 24 hours, adverse effects, and parents satisfaction.Timepoint: intraoperatively after administration of the block and at 30,60,90,120min,6,12 and 24hours postoperatively.

Countries

India

Contacts

Public ContactKrishna Rao Maremanda

Nizams Institute of Medical Sciences

maremanda.krishnarao@gmail.com8790615789

Outcome results

None listed

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