Multi Centre Study on TESS V2 Shoulder System

Status Completed

Clinical Trial Summary

This study is a Post Market Clinical Follow-up study to fulfill the post market surveillance requirements. The data collected from this study will serve the purpose of confirming safety and performance of the TESS Shoulder System.

Clinical Trial Description

The objective of this retrospective and prospective, multicenter, non-controlled Post Market Clinical Follow-up study is to evaluate the mid-term (5-year) clinical performance of the TESS Version 2 Anatomic and Reverse prostheses in shoulder arthroplasty. The primary outcome is defined as the clinical performance determined using Constant Score. The secondary outcomes are the passive and active mobility, the radiographic evaluation, the complications (including dislocation and revisions/removals) and survivorship. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03431857
Study type	Observational
Source	Zimmer Biomet
Contact
Status	Completed
Phase
Start date	October 20, 2010
Completion date	December 31, 2019

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