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Clinical Trial Summary

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


Clinical Trial 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 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03828916
Study type Interventional
Source NuTech Medical, Inc
Contact Katie Mowry
Phone 205-800-8301
Email kmowry@organo.com
Status Recruiting
Phase N/A
Start date January 30, 2019
Completion date June 2021

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