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Persona OsseoTi Keel Compatibility Study (Total Knee Arthroplasty)

NCT05787821 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 760

Last updated 2026-01-20

No results posted yet for this study

Summary

The main objective of the study is to evaluate the safety, performance and clinical benefits of the Persona implant and its instrumentation in primary total knee arthroplasty

Conditions

  • Knee Pain Chronic
  • Osteoarthritis, Knee
  • Rheumatoid Arthritis
  • Traumatic Arthritis
  • Polyarthritis
  • Varus Deformity
  • Valgus Deformity
  • Flexion Deformity of Knee
  • Avascular Necrosis

Interventions

DEVICE

Total Knee Arthroplasty

Total knee replacement.

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Hillary Overholser · Zimmer Biomet

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-28
Primary Completion
2026-06-30
Completion
2035-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05787821 on ClinicalTrials.gov