New knee implant tracked for 5 years in 777 patients
NCT ID NCT02337244
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 777 adults aged 18-75 who received the Persona Total Knee System to treat severe knee pain and disability from conditions like osteoarthritis or rheumatoid arthritis. Researchers will track how long the implant lasts, how safe it is, and how well it improves pain and function over 5 years. The goal is to gather real-world data on the implant's performance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Zimmer Persona Total Knee System (artificial knee implant)
- What this could lead to
- If successful, this could confirm that the Persona knee implant provides long-lasting pain relief and improved function for people with severe knee arthritis.
- What could go wrong
- This is an observational study, not a controlled trial, so results may not prove the implant is better than other options. Some patients may still experience complications like implant loosening or infection.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
777 people
The number who actually took part.
- Started
-
Nov 2013
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Primary total knee arthroplasty subjects that receive the Zimmer Persona Total Knee System.
- Ages
-
18 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient 18-75 years of age, inclusive. * Patient qualifies for primary total knee arthroplasty based on physical exam and medical history, including diagnosis of severe knee pain and disability due to at least one of the following: * rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis; * collagen disorders and/or avascular necrosis of the femoral condyle; * post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy; * moderate valgus, varus, or flexion deformities; * the salvage of previously failed surgical attempts that did not include partial or total knee arthroplasty of the ipsilateral knee. * Patient is willing and able to complete scheduled study procedures and follow-up evaluations. * Independent of study participation, patient is a candidate for commercially available Zimmer Persona knee implants implanted in accordance with product labeling. Exclusion Criteria: * Patient is currently participating in any other surgical intervention studies or pain management studies. * Previous history of infection in the affected joint and/or other local/systemic infection that may affect the prosthetic joint. * Insufficient bone stock on femoral or tibial surfaces. * Skeletal immaturity. * Neuropathic arthropathy. * Osteoporosis or any loss of musculature or neuromuscular disease that compromises the affected limb. * Stable, painless arthrodesis in a satisfactory functional position. * Severe instability secondary to the absence of collateral ligament integrity. * Rheumatoid arthritis accompanied by an ulcer of the skin or a history of recurrent breakdown of the skin. * Patient has a known or suspected sensitivity or allergy to one or more of the implant materials. * Patient is pregnant or considered a member of a protected population (e.g., prisoner, mentally incompetent, etc.). * Patient has previously received partial or total knee arthroplasty for the ipsilateral knee.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Osteoarthritis are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Atos Klinik Heidelberg
Heidelberg, Germany
-
CHU de Clermont-Ferrand
Clermont-Ferrand, 63003, France
-
Centre Hospitalier régional Universitaire de Montpellier
Montpellier, 34980, France
-
Golden Jubilee National Hospital
Clydebank, United Kingdom
-
HEH Braunschweig
Braunschweig, Germany
-
Harrogate and District NHS
Harrogate, HG2 7SX, United Kingdom
-
Hospital Miguel Servet
Zaragoza, Spain
-
Hospital Parc Tauli
Sabadell, Spain
-
Orthopädisches Spital Speising
Vienna, 1130, Austria
-
Stichting Research Orthopedie & Reinier de Graaf Groep
Delft, 2612, Netherlands
-
The Newcastle Upon Tyne Hospitals
Newcastle, United Kingdom
-
University of Leeds
Leeds, Leeds/UK, LS2 9JT, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Scientists probe why rheumatic pain feels different for everyone
- Custom knee guides put to the test in obese patients
- A new ankle? researchers track 400 people with an implant meant to restore movement
- Can a Job-Focused rehab program keep arthritis patients employed?
- Surgeons test augmented reality to Fine-Tune knee replacement cuts
- Do rheumatic diseases quietly damage the Eye's oil glands?