Using guided growth to manage increased femoral anteversion in children
Role of Rotational Guided Growth in Management of Increased Femoral Anteversion
This study tests if a new method to guide bone growth can help children with a condition called increased femoral anteversion, making their legs straighter and reducing any related problems.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 15 (estimated) |
| Ages | 8 Years to 16 Years |
| Sex | All |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo, El-Waily) |
| Trial ID | NCT06320769 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of rotational guided growth techniques in correcting increased femoral anteversion in children. It aims to assess the clinical and radiographic outcomes of different constructs used in the procedure. Additionally, the study will monitor potential complications such as limb length discrepancy and other deformities. The approach builds on previous animal and limited human studies that have explored similar methodologies.
Who should consider this trial
Good fit: Ideal candidates are children aged 8 years and older with increased femoral anteversion leading to in-toeing and decreased agility.
Not a fit: Patients who have previously undergone femoral osteotomy or have conditions like cerebral palsy or skeletal dysplasias will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could provide a less invasive option for correcting rotational deformities in children, improving mobility and quality of life.
How similar studies have performed: Previous studies have shown promise in using guided growth for similar conditions, but this specific approach is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Children with increased femoral anteversion causing in-toeing with decreased agility. * Aged 8 years and above with at least two years of bone growth remaining. Exclusion Criteria: * Any patient who underwent previous femoral osteotomy. * Any patient with sick physis (skeletal dysplasias, post traumatic / post infective physeal damage, active rickets). * Cerebral Palsy (CP) patients
Where this trial is running
Cairo, El-Waily
- Faculty of Medicine, Ainshams University — Cairo, El-Waily, Egypt (Recruiting)
Study contacts
- Study coordinator: Ahmed Mohamed Mohamed Abdelghany Badr, Msc
- Email: abaghany@gmail.com
- Phone: +201060085397
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.