Investigating MPFL reconstruction outcomes in children
Medial Patellofemoral Ligament Reconstruction in Children - a 2-8 Years Follow-up Study
This study looks at how well MPFL reconstruction surgery works for children with knee problems over several years compared to healthy kids.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 160 (estimated) |
| Ages | 14 Years to 23 Years |
| Sex | All |
| Sponsor | Aarhus University Hospital Academic / other |
| Locations | 1 site (Aarhus N) |
| Trial ID | NCT06257836 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the long-term outcomes of medial patellofemoral ligament (MPFL) reconstruction in children suffering from chronic patellar instability. The study will involve a cohort of children who have undergone MPFL reconstruction using autologous tendon tissue and will compare their outcomes with a healthy control group matched by age and gender. The focus is on assessing the effectiveness of the surgical intervention over a follow-up period of 2 to 8 years. The study will also consider various factors that may influence the success of the reconstruction.
Who should consider this trial
Good fit: Ideal candidates for this study are children with chronic patellar instability who are undergoing MPFL reconstruction.
Not a fit: Patients who have had multiple surgeries on the same knee or a revision of MPFL in the index knee may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness of MPFL reconstruction in improving knee stability and function in children.
How similar studies have performed: Other studies have shown promising results with MPFL reconstruction techniques, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria - Intervention group: * MPFL-reconstruction with Quadriceps tendon graft * Open physis at surgery date * Minimum 2 years Follow up Exclusion Criteria - Intervention group: * More surgeries in index knee * MPFL-r in opposite knee * MPFL revision in index knee Inclusion Criteria - Healthy group: * No knee problems Exclusion Criteria - Healthy group * None * No knee problems
Where this trial is running
Aarhus N
- Division of Sports Trauma, Palle Juul-Jensens Boulevard 99 — Aarhus N, Denmark (Recruiting)
Study contacts
- Study coordinator: Torsten G Nielsen, MHSc
- Email: torsne@rm.dk
- Phone: +4540491184
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.