Assessing nerve function after fibular epiphyseal transfer in children
Peroneal Nerve Dysfunction in Proximal Fibular Epiphyseal Harvesting Cases
This study looks at how surgery on the fibula affects nerve function in children to see if keeping blood flow to the growth plate can help prevent nerve damage.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 15 (estimated) |
| Ages | 18 Months to 14 Years |
| Sex | All |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Assiut) |
| Trial ID | NCT05884827 on ClinicalTrials.gov |
What this trial studies
This observational study evaluates peroneal nerve dysfunction following proximal fibular epiphyseal resection in children. It focuses on assessing clinical outcomes and electromyography (EMG) changes post-surgery. The study aims to understand the relationship between the preservation of vascularity in the growth plate and the potential risk of nerve damage during the procedure. By analyzing these factors, the research seeks to improve surgical techniques and patient outcomes in cases of epiphyseal arrest.
Who should consider this trial
Good fit: Ideal candidates for this study include children with traumatic bone defects, congenital malformations, malignant bone lesions, or infections requiring epiphyseal transfer.
Not a fit: Patients who do not have any injury to the nerve supply of the tibialis anterior during surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques that minimize nerve damage and enhance recovery in children undergoing epiphyseal transfer.
How similar studies have performed: While there may be limited studies specifically addressing this approach, the evaluation of nerve function in similar surgical contexts has shown promise in improving patient outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * all patients candidate for epiphyseal transfer are included ( patients with traumatic bone defect, congenital malformations, malignant bone lesions and infection ) Exclusion Criteria: * patients in which there's no injury of nerve supply of tibialis anterior has occurred intraoperative
Where this trial is running
Assiut
- Omar — Assiut, Egypt (Recruiting)
Study contacts
- Study coordinator: Ahmed Moustafa Elsese, Resident
- Email: Ahmedelsese@med.aun.edu.eg
- Phone: 01009246781
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.