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Embody Insertional Achilles Tendinopathy — IAT  

Insertional Achilles Tendinopathy Clinical Trial

Official title:
A Multi-Center, Prospective Case Series Evaluating Insertional Achilles Tendinopathy Repair Augmented With TAPESTRY® Biointegrative Implant

Clinical Trial Summary

The primary objective of this study is to evaluate the long-term effects on ankle/Achilles tendon pain after repair of insertional Achilles tendinopathy (IAT) augmented with TAPESTRY Biointegrative Implant.

Clinical Trial Description

This study is a prospective case series of patients who have had insertional Achilles tendinopathy repair augmented with the Tapestry Biointegrative Implant. The primary aim of the study is to describe patient reported pain 12 months after surgical repair with Tapestry. The secondary aims are to assess the proportion of study subjects that experience treatment-related adverse events post-surgery, treatment related serious adverse events resulting in second surgical intervention, quality of life and other patient reported outcomes at all follow up timepoints post-surgery, and tissue thickness measured with MRI at 6 months post-surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05998785
Study type Observational
Source Zimmer Biomet
Contact
Status Suspended
Phase
Start date August 2, 2022
Completion date December 2024
View Details
See also
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