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Orthopedic Implant

Persona TM Tibia subjects for Joint Dislocation

N/A
Waitlist Available
Research Sponsored by Zimmer Biomet
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights

Study Summary

This study is evaluating whether a new type of knee replacement is as good as the current standard.

Eligible Conditions
  • Joint Dislocation
  • Osteoarthritis
  • Polyarthritis
  • Bow Legs or Knock Knees
  • Rheumatoid Arthritis
  • Osteonecrosis of the Femoral Condyle

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Radiograph assessment of progressive tibial radiolucencies
Secondary outcome measures
Oxford Knee Score
Revision Rate

Trial Design

1Treatment groups
Experimental Treatment
Group I: Persona TM Tibia subjectsExperimental Treatment1 Intervention
Subjects that receive the Persona TM Tibia implant
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Persona TM Tibia
2018
N/A
~170

Find a Location

Who is running the clinical trial?

Zimmer BiometLead Sponsor
373 Previous Clinical Trials
67,236 Total Patients Enrolled
Kacy Arnold, RN, MBAStudy DirectorZimmer Biomet
15 Previous Clinical Trials
3,841 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~23 spots leftby Apr 2025