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Clinical Trial Summary

The objectives of this study are to confirm safety and performance of the Anatomical Shoulder Domelock System when used in hemi or total shoulder arthroplasty by analysis of standard scoring systems, radiographs and adverse event records.


Clinical Trial Description

This study is a multicenter, prospective and retrospective, non-controlled PMCF study involving orthopaedic surgeons skilled in hemi and total shoulder arthroplasty procedures. A minimum of six study centers will be involved and a total number of 73 implants will be included into the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03312465
Study type Observational
Source Zimmer Biomet
Contact
Status Active, not recruiting
Phase
Start date September 28, 2017
Completion date December 31, 2033

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