Outcomes in Rotator Cuff Repair Using Graft Reinforcement

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate patient shoulder functional outcomes following rotator cuff repairs reinforced with a surgical mesh.

Clinical Trial Description

Conexa is a surgical mesh derived from porcine dermis and processed to produce an acellular dermal matrix. It is designed to perform as a surgical mesh for use as a soft tissue patch to reinforce soft tissue where weaknesses exist and for the surgical repair of damaged or ruptured soft tissue membranes. The purpose of this post-market clinical study is to collect safety and efficacy data when Conexa is used to repair torn tendons of the rotator cuff. Conexa will be used in accordance with its labeling for this clinical study. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Rotator Cuff Tear

Clinical Trial Details

NCT number	NCT01025037
Study type	Interventional
Source	Tornier, Inc.
Contact
Status	Completed
Phase	N/A
Start date	October 2009
Completion date	April 2014

View Details

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