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To Evaluate the Performance of the CORI™ KNEE TENSIONER as an Accessory to the CORI™ Surgical System.

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NCT04849884 · results posted

Sponsored by Smith & Nephew, Inc. (industry) · SNN — their whole pipeline →.

Phase
Not applicable
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
77actual
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
DateFiledBasisWhat it is
Start2022-03-30actualWhen the study began enrolling
Primary completion2025-06-04actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-06-04actualThe whole study's end, after follow-up
First posted2021-04-19actualWhen this record first appeared on the registry
Results posted2026-06-30actualWhen the sponsor posted results to the registry
Record updated2026-06-30actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Arthroplasty
  • Replacement
  • Knee

Intervention

  • Device: CORI™ KNEE TENSIONER

Primary outcome

what the primary-completion date above is the date OF
EuroQol 5-Dimension 5-Level Visual Analogue Scale (EQ-5D-5L VAS) Score Change From Baseline to 6 Weeks, 6 Months, and 12 Months
measured Baseline, 6 weeks, 6 months, 12 months

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2025-03-05 · 3.2 MB · Prot_000.pdf
Statistical Analysis Planposted 2025-08-12 · 976 KB · SAP_001.pdf

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