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Orthopedic Implant
Titanium Knee Implant for Knee Arthritis (TKA Trial)
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
Patient is of legal age and skeletally mature
Patient qualifies for total knee arthroplasty based upon physical exam and medical history, and meets the approved indications for use of the Persona Ti-Nidium Knee System and Vivacit-E polyethylene articulating surface
Must not have
Patient is unwilling to sign the Informed Consent
Patient is institutionalized or is a known drug abuser, a known alcoholic or cannot understand the requirements of study participation
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 10 years
Awards & highlights
No Placebo-Only Group
Summary
This trial evaluates the safety and effectiveness of the Persona Ti-Nidium implant in patients needing knee replacement surgery. The implant aims to improve movement and reduce pain by replacing damaged knee parts with an artificial joint. The study will follow patients for several years to assess long-term outcomes. The Persona® system is a newly launched implant designed for total knee replacement with innovations intended for better function and higher flexibility.
Who is the study for?
This trial is for adults with various knee conditions like osteoarthritis, rheumatoid arthritis, and chronic knee pain who need a total knee replacement. Participants must be able to consent and follow the study's procedures. Those with mental conditions affecting treatment adherence or at high risk as determined by the investigator are excluded.
What is being tested?
The Persona Ti-Nidium Total Knee System is being tested for its effectiveness and safety in total knee arthroplasty (knee replacement surgery). The study aims to assess how well this implant works over time in patients undergoing surgery.
What are the potential side effects?
While not explicitly listed, potential side effects may include pain at the surgical site, swelling, infection risks associated with surgeries, issues with implant fitting or durability, and possible allergic reactions to materials.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am an adult and my bones have stopped growing.
Select...
I am eligible for a knee replacement using specific materials based on my medical history and physical exam.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am not willing to sign the Informed Consent.
Select...
I am not institutionalized, a known drug abuser, alcoholic, and I understand the study requirements.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 10 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~10 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Oxford Knee Score (OKS)
Secondary study objectives
EuroQol Five Dimension Five Level (EQ-5D-5L) Outcomes Measure
Knee Society Score (KSS) Expectations (pre and post op)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Persona Ti-NidiumExperimental Treatment1 Intervention
Primary total knee arthroplasty subjects that receive the Zimmer Biomet Persona Ti-Nidium Total Knee System
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for osteoarthritis (OA) include nonsteroidal anti-inflammatory drugs (NSAIDs), glucocorticoids, and joint replacement surgery. NSAIDs, such as ibuprofen and naproxen, work by reducing inflammation and pain through the inhibition of cyclooxygenase enzymes (COX-1 and COX-2).
Glucocorticoids, like prednisone, provide anti-inflammatory effects by suppressing the immune response and reducing inflammation in the joints. Joint replacement surgery, such as the Persona Ti-Nidium implant in total knee arthroplasty (TKA), involves replacing the damaged joint surfaces with artificial components, which helps restore function and alleviate pain.
These treatments are crucial for OA patients as they address pain management, improve joint function, and enhance the quality of life.
Non-pharmacological and non-surgical interventions to manage patients with knee osteoarthritis: An umbrella review.
Non-pharmacological and non-surgical interventions to manage patients with knee osteoarthritis: An umbrella review.
Find a Location
Who is running the clinical trial?
Zimmer BiometLead Sponsor
375 Previous Clinical Trials
67,293 Total Patients Enrolled
135 Trials studying Osteoarthritis
34,347 Patients Enrolled for Osteoarthritis
Hillary OverholserStudy DirectorZimmer Biomet Assoc Director
12 Previous Clinical Trials
2,853 Total Patients Enrolled
8 Trials studying Osteoarthritis
2,070 Patients Enrolled for Osteoarthritis
Kacy Arnold, RN, MBAStudy DirectorClinical Affairs Director
15 Previous Clinical Trials
3,749 Total Patients Enrolled
12 Trials studying Osteoarthritis
3,482 Patients Enrolled for Osteoarthritis
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am eligible for a specific knee replacement surgery.I am willing and able to follow the study's schedule for check-ups.I am not willing to sign the Informed Consent.I am an adult and my bones have stopped growing.I am eligible for a knee replacement using specific materials based on my medical history and physical exam.I am not institutionalized, a known drug abuser, alcoholic, and I understand the study requirements.
Research Study Groups:
This trial has the following groups:- Group 1: Persona Ti-Nidium
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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