Biologic Augment of the Medial Patellofemoral Ligament Following Primary Lateral Patellofemoral Dislocation (BioPPD)
Recruiting
N/A
Interventional Study
Patellofemoral Dislocation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 13 – 30
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 20 (estimated)
- Sponsor
- Banff Sport Medicine Foundation · Other
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About This Trial
This study aims to determine the ability of medial patellofemoral ligament (MPFL) repair augmented with Biobrace® to decrease the re-dislocation rate after a primary patellofemoral dislocation. First-time patellofemoral dislocation is a significant problem, and the ramifications of recurrence for patients are substantial. Due to the multifactorial nature of the pathoanatomy of patellofemoral insta…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 13 - 30 years
* First-time lateral patellofemoral dislocation in the previous 7 days
* Closed or closing growth plates (confirmed on knee x-rays with no change required for surgical technique)
Exclusion Criteria:
* History of previous patellofemoral dislocation on the in…
Contacts