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RecruitingNCT07023094

PENG With LFCB vs. ESP Blocks for Pediatric Hip Surgery

Comparison of Analgesic Efficacy of Pericapsular Nerve Group (PENG) Block With Lateral Femoral Cutaneous Nerve Block (LFCB) Versus Lumbar and Sacral Erector Spinae Plane Blocks (L-ESPB and S-ESPB) in Pediatric Hip Surgery: A Randomized Controlled Trial

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Poznan University of Medical Sciences · Academic / Other
Sex
All
Age
2 Years – 16 Years
Healthy volunteers
Not accepted

Summary

This randomized controlled trial (RCT) compares the analgesic effectiveness of two regional anesthesia techniques-Pericapsular Nerve Group (PENG) block combined with Lateral Femoral Cutaneous Nerve Block (LFCB) versus Lumbar and Sacral Erector Spinae Plane Blocks (L-ESPB and S-ESPB)-in pediatric patients undergoing hip surgery.

Detailed description

Orthopedic hip procedures in pediatric patients, including osteotomies, arthroscopic interventions, and reconstructive surgeries, often result in significant postoperative pain. Effective analgesia is critical for reducing surgical stress, accelerating rehabilitation, and minimizing opioid use and associated side effects. Regional anesthesia techniques have gained attention for their opioid-sparing effects and enhanced recovery profiles. This randomized controlled trial aims to compare the analgesic effectiveness of two regional anesthetic approaches: \- The pericapsular nerve group (PENG) block is combined with the lateral fetal cutaneous nerve block (LFCB), targeting hip joint innervation directly and providing comprehensive sensory coverage. Lumbar and sacral erector spinae plane blocks (L-ESPB and S-ESPB) employ fascial plane techniques to deliver analgesia by diffusing local anesthetic around nerves innervating the hip region. This trial aims to establish the optimal regional anesthesia technique and determine the clinical benefits of using dexamethasone and dexmedetomidine as adjuvants. The results will guide clinicians toward evidence-based analgesic protocols in pediatric orthopedic hip surgery, potentially reducing opioid-related complications and improving patient recovery outcomes.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine 0.2% for PENG BlockU-S guided PENG (0.4 mL/kg) with 0.2% ropivacaine
DRUGRopivacaine 0.2% for LFCBLFCB (0.1 mL/kg) with 0.2% ropivacaine
DRUGRopivacaine 0.2% for L-ESPBLumbar ESPB (0.25ml/kg) with 0.2% ropivacaine
DRUGRopivacaine 0.2% for S-ESPBSacral ESPB (0.25ml/kg) with 0.2% ropivacaine

Timeline

Start date
2025-06-16
Primary completion
2026-05-30
Completion
2026-06-30
First posted
2025-06-15
Last updated
2025-07-11

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT07023094. Inclusion in this directory is not an endorsement.