Comparing two types of nerve blocks for hip dysplasia surgery in children
Pericapsular Nerve Group Block Combined Versus Trans Muscular Quadratus Lumborum Block in Pediatric Patients Undergoing Correction of Dysplasia of the Hip: a Prospective Randomized Double Blinded Study
NA · Cairo University · NCT06130761
This study is testing which of two different nerve block techniques can better manage pain for children having surgery for hip dysplasia.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 6 Months to 6 Years |
| Sex | All |
| Sponsor | Cairo University (other) |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06130761 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the analgesic effects of two different nerve block techniques—pericapsular nerve group block combined with lateral femoral cutaneous nerve block and trans muscular quadratus lumborum block—in pediatric patients undergoing surgical repair for developmental dysplasia of the hip. Patients will be monitored with standard anesthesia protocols and randomly assigned to one of the two intervention groups. The nerve blocks will be performed under ultrasound guidance to ensure accuracy and effectiveness in pain management during and after the surgery.
Who should consider this trial
Good fit: Ideal candidates are children aged 6 months to 6 years scheduled for surgical repair of developmental dysplasia of the hip.
Not a fit: Patients with severe comorbidities (ASA III or IV), infections at the block site, or allergies to local anesthetics may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for children undergoing hip dysplasia surgery.
How similar studies have performed: Other studies have shown promising results with similar nerve block techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Acceptance of the parents 2. Children of both gender 3. ASA I \& ASA II 4. Age ranging between 6 months up to 6years old (neglected cases) 5. Scheduled to DDH surgical repair (open reduction or osteotomy) either unilateral or bilateral. 6. Revision cases. Exclusion Criteria: 1. Parent refusal 2. ASA III, IV 3. Infection at site of block 4. History of allergy to local anesthetics 5. Bleeding disorders with INR \> 1.5 and/or platelets \< 100,000/mm3
Where this trial is running
Cairo
- Anesthesia Department, Kasralainy Faculty of Medicine, Cairo University. — Cairo, Egypt (RECRUITING)
Study contacts
- Study coordinator: Mahmoud R Sewilam, Lecturer
- Email: mr.sewilam@gmail.com
- Phone: +201008855731
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Hip Dysplasia, quadratus lumborum blocks