Comprehensive Reverse Shoulder Data Collection
← catalyst calendarNCT03404778 · readout ≤ 134 d
Sponsored by Zimmer Biomet (industry) · ZBH — their whole pipeline →.
Phase
—
Status
Enrolling by invitation
Study type
Observational
Enrollment
175estimated
Sites
4
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2010-03-07 | actual | When the study began enrolling |
| Primary completion | Dec 2026 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | Dec 2036 | estimated | The whole study's end, after follow-up |
| First posted | 2018-01-19 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-10-30 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Arthropathy of Shoulder Region
- Grossly Deficient Rotator Cuff
- Osteoarthritis of the Shoulder
- Rheumatoid Arthritis Without Humeral Metaphyseal Defects
- Post-Traumatic Arthitis
Intervention
- Device: Biomet Comprehensive Reverse Shoulder
Primary outcome
what the primary-completion date above is the date OFPain Score
measured 1 year
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