Last updated on January 2020

NuShield in Surgical Peroneal Tendon Repair


Brief description of study

The purpose of this study is to evaluate the use of NuShield in subjects requiring surgical tendon repair.

Detailed Study Description

The objective of this clinical trial is to evaluate both the safety and efficacy of using the NuShield allograft in addition to standard of care surgical procedures in subjects requiring surgical repair of the peroneal tendon. The effects of this treatment will be assessed using:

  • Questionnaires
  • Visual Analog Scale Foot and Ankle (VAS FA)
  • FAAM Sport
  • PROMIS Global Health SF
  • Tegner Activity Scale
  • Foot and Ankle Outcomes Instrument (Q1, Q2)
  • Swelling assessments
  • Ultrasound imaging for tendon thickness, gliding and adhesion formation

Clinical Study Identifier: NCT03828916

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