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Clinical trial

Post-market Clinical Follow-up Study to Provide Safety, Performance and Clinical Benefits Data of the Comprehensive Versa-Dial Reverse Titanium (Ti) Glenosphere in Primary, Fracture and Revision Total Shoulder Arthroplasty

NCT04003272 is registered in ClinicalTrials.gov with Zimmer Biomet as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Post-market Clinical Follow-up Study to Provide Safety, Performance and Clinical Benefits Data of the Comprehensive Versa-Dial Reverse Titanium (Ti) Glenosphere in Primary, Fracture and Revision Total Shoulder Arthroplasty
Lead sponsor
Zimmer Biomet
Phase
Observational
Overall status
Enrolling by invitation
Start date
October 28, 2019
Completion date
September 1, 2035
Enrollment
59 (estimated)
Sites
2

Conditions

As the registry lists them; a condition with its own page is linked.

shoulder arthritis, shoulder disease, shoulder fractures, shoulder injuries, shoulder pain