ROSA® Knee System V1.5 Pilot Study
← catalyst calendarSponsored by Zimmer Biomet (industry) · ZBH — their whole pipeline →.
Phase
Not applicable
Status
Completed
Study type
Interventional
Design
Na · None · Other
Enrollment
40actual
Sites
1
Country
New Zealand
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 | 2025-02-25 | actual | When the study began enrolling |
| Primary completion | 2026-02-17 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2026-02-17 | actual | The whole study's end, after follow-up |
| First posted | 2025-06-08 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-02-27 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Knee Arthroplasty, Total
- Robotic Surgical Procedures
- Joint Diseases
- Knee Osteoarthritis
Intervention
- Device: Total Knee Arthroplasty
Primary outcome
what the primary-completion date above is the date OFIncidence of Procedure-Emergent Adverse Events, to assess the Safety of the ROSA® Knee System v1.5 System
measured Intra-operative observations, with immediate post-operative documentation and reporting period.
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