Achilles Tendon Repair With Bioinductive Implant

Status Completed

Clinical Trial Summary

To evaluate bioinduction of new tissue and tendon healing after implantation of the Rotation Medical Bioinductive Implant used as adjunct to surgical repair in the treatment of insertional Achilles tendonitis.

Clinical Trial Description

This is a prospective, non-randomized, single-arm study conducted under a common protocol designed to evaluate long-term outcomes following open treatment and implantation of the Rotation Medical Bioinductive Implant to treat insertional Achilles tendinopathy. Up to 20 subjects will be enrolled and treated with the Rotation Medical Bioinductive Implant. Enrollment is anticipated to take up to 12 months and all subjects will be followed for two years after surgery. Therefore, the overall study duration is estimated to be 36 months. ;

Study Design

Related Conditions & MeSH terms

Tendinopathy

Clinical Trial Details

NCT number	NCT02811003
Study type	Interventional
Source	Smith & Nephew, Inc.
Contact
Status	Completed
Phase	N/A
Start date	June 3, 2016
Completion date	September 17, 2019

View Details

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