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Study identifier: NCT06169800 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Biologic Augment of the Medial Patellofemoral Ligament Following Primary Lateral Patellofemoral Dislocation (BioPPD)

Condition: Patellofemoral Dislocation  ·  Sponsor: Banff Sport Medicine Foundation

PhaseNA
Planned participants20
Who can joinAll sexes, 13 Years to 30 Years
Healthy volunteersNo

About this study

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 instability, it has been difficult to design trials that will show how interventions could affect the natural history of these young patients. No definitive studies have determined whether the surgical reconstruction of the MPFL in patients with mild to moderate pathoanatomic risk factors will decrease the re-dislocation rate after a first-time dislocation. In addition, to date, no synthetic option has provided both biology and strength for ligament augmentation. This innovation may allow for a minimalist approach to keeping the patella centred in the trochlear groove during the healing phase after a first-time dislocation.

This description comes directly from the study's public registry record.

Talk to the study team

Laurie A Hiemstra, MD, PhD  ·  403 760 2897  ·  research@banffsportmed.ca

Sarah Kerslake, BPT  ·  403 760 2897  ·  sarah@banffsportmed.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Banff Sport MedicineCanmore, Alberta, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06169800