Trials / Recruiting
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
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine 0.2% for PENG Block | U-S guided PENG (0.4 mL/kg) with 0.2% ropivacaine |
| DRUG | Ropivacaine 0.2% for LFCB | LFCB (0.1 mL/kg) with 0.2% ropivacaine |
| DRUG | Ropivacaine 0.2% for L-ESPB | Lumbar ESPB (0.25ml/kg) with 0.2% ropivacaine |
| DRUG | Ropivacaine 0.2% for S-ESPB | Sacral 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.