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Persona Total Knee Arthroplasty Outcomes Study

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. 4 versions Re-verified since Aug 27, 2023, no change to tracked fieldsv18-v21
  2. Trial status: Recruiting to Active, Not Recruiting Enrollment target: estimated 1000 to confirmed 737 · Site details revised at 14 of 14 sitesv17 Show 2 more changesShow less
    • Enrollment target: estimated 1000 to confirmed 737
    • Site details revised at 14 of 14 sites
  3. Site details revised at 1 of 14 sitesv16
  4. Re-verified, no change to tracked fieldsv15
  5. Site details revised at 2 of 14 sitesv14
Show 12 earlier versionsHide 12 earlier versions
  1. Secondary endpoints: details revised at 1 of 1 entry Site details revised at 2 of 14 sitesv13 Show 1 more changeShow less
    • Site details revised at 2 of 14 sites
  2. Study sites: 13 to 14v12
  3. Site details revised at 4 of 13 sites Study arms: 0 to 1v11 Show 1 more changeShow less
    • Study arms: 0 to 1
  4. Phase: Not specified to Not applicablev10
  5. Re-verified, no change to tracked fieldsv9
  6. Site details revised at 3 of 13 sitesv8
  7. Study sites: 12 to 13v7
  8. Study sites: 11 to 12v6
  9. Study sites: 10 to 11v5
  10. Study sites: 8 to 10v4
  11. Study sites: 7 to 8v3
  12. Study sites: 5 to 7v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The primary objective of this study is to obtain implant survivorship and clinical outcomes data for commercially available Persona fixed bearing knee implants used in total knee arthroplasty. The assessment will include implant survivorship and clinical performance.
Trial Details
NCT Number NCT02255383
Lead Sponsor Zimmer Biomet
Conditions Knee Pain Chronic, Osteoarthritis, Rheumatoid Arthritis, Traumatic Arthritis, Polyarthritis, Moderate Varus, Valgus or Flexion Deformities, Avascular Necrosis of the Femoral Condyle
Enrollment 737 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov