Tendinopathy Clinical Trial
Official title:
Single Arm Clinical Evaluation of the Safety and Efficacy of the NuShield® Allograft for Peroneal Tendon Repair
The purpose of this study is to evaluate the use of NuShield in subjects requiring surgical tendon repair.
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
;
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