Southfield, MINCT04821154Now EnrollingIRB Ready

Arthroplasty Complications Clinical Trial in Southfield, MI

Access cutting-edge arthroplasty complications treatment through this clinical trial at a research site in Southfield. Study-provided care at no cost to qualified participants.

Sponsored by Zimmer Biomet

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Expert Care in Southfield

Access arthroplasty complications specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related arthroplasty complications treatment provided free

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Check if you qualify for this arthroplasty complications clinical trial in Southfield, MI

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Southfield

    Convenient for MI residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Southfield site if eligible
  4. 4Begin participation

About This Arthroplasty Complications Study in Southfield

The study will evaluate the performance, clinical benefits and safety of the Persona Revision Knee System in patients who have received primary or revision total knee arthroplasty (TKA) treatment. This will be done using a multicenter, single-arm, consecutive series, retrospective cohort study with prospective follow-up.

Sponsor: Zimmer Biomet

Who Can Participate

Inclusion Criteria

Male or female of at least 18 years of age at the time of screening.
Signed an institutional review board approved informed consent.
Willingness and ability to comply with the study procedures and visit schedules and ability to understand and follow oral and written post-operative care instructions.
Previous medical diagnosis/ history of at least one of the following conditions requiring treatment using the Persona Revision Knee System within a pre-specified study variant configuration (cohort), in accordance with the instructions for use (IFU):
Rheumatoid arthritis, osteoarthritis, traumatic arthritis or 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 or for a knee in which satisfactory stability in flexion cannot be obtained at the time of surgery
A pre-operative Knee Society Knee Score (objective assessment) ≤ 80.

Exclusion Criteria

1\) Presence of clinically observed active or suspected latent infection in the affected joint at the time of procedure. 3\) Presence of of local/systemic/distant focal infection that may affect or hematogenously spread to the prosthetic joint. 4\) Skeletal immaturity or insufficient bone stock on femoral or tibial surfaces which cannot provide adequate support and/or fixation to the prosthesis. 5\) Diagnosed with neuropathic arthropathy, osteoporosis, or any loss of musculature or neuromuscular disease that compromises the affected limb. 6\) Presence of a stable, painless arthrodesis in a satisfactory functional position in the affected joint. 7\) Severe instability of the affected joint secondary to the absence of collateral ligament integrity. 8\) Diagnosis of rheumatoid arthritis in conjunction with any of the following at the time of screening:
An ulcer of the skin
History of recurrent breakdown of the skin
Use of steroids 9\) Patient requires simultaneous bilateral knee surgery for treatment of diagnosed condition. 10\) Pregnant or women planning to become pregnant during the time they will be participating in the study. 11\) Any documented clinically significant degree of cognitive impairment or other condition, finding, or psychiatric illness at screening which, in the opinion of the Investigator, could compromise patient safety or interfere with the assessment of the safety and treatment effects of the study procedure. 12\) Any patient who is institutionalized, or with a known drug or alcohol dependence currently or within the last year.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Southfield?

Yes, this clinical trial (NCT04821154) has an active research site in Southfield, MI that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Arthroplasty Complications Treatment Options in Southfield, MI

If you're searching for arthroplasty complications treatment options in Southfield, MI, this clinical trial (NCT04821154) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Southfield research site is actively enrolling participants for this clinical trial. You'll receive care from experienced arthroplasty complications specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all arthroplasty complications clinical trials near you to find additional studies recruiting in your area.

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