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Clinical Trial Summary

The objectives of this study are to confirm safety, performance and clinical benefits of the Anaverse™ Glenoid System and its instrumentation by analysis of standard scoring systems, radiographs and adverse event records.


Clinical Trial Description

The safety of the system will be assessed by monitoring the frequency and incidence of adverse events. The performance and clinical benefits will be evaluated by assessment of the overall pain and functional performance, survival, and radiographic parameters of all enrolled study subjects. The primary endpoint is defined by the survival of the implant system at 2 years which is based on removal or intended removal of the Anaverse™ Glenoid System baseplate and will be determined by using the Kaplan Meier method. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05215600
Study type Observational
Source Zimmer Biomet
Contact
Status Active, not recruiting
Phase
Start date May 6, 2022
Completion date June 2024

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