Spartanburg, SCNCT06040827Now EnrollingIRB Ready

Knee Osteoarthritis Clinical Trial in Spartanburg, SC

Access cutting-edge knee osteoarthritis treatment through this clinical trial at a research site in Spartanburg. Study-provided care at no cost to qualified participants.

Sponsored by Canary Medical

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Expert Care in Spartanburg

Access knee osteoarthritis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related knee osteoarthritis treatment provided free

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Check if you qualify for this knee osteoarthritis clinical trial in Spartanburg, SC

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Spartanburg

    Convenient for SC 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 Spartanburg site if eligible
  4. 4Begin participation

About This Knee Osteoarthritis Study in Spartanburg

The objectives of this prospective observational cohort study are to evaluate the safety, reliability, reproducibility, and accuracy of the Canary canturioTM te post-TKA.

Sponsor: Canary Medical

Who Can Participate

Inclusion Criteria

Patient must be 18 years of age or older
Patient qualifies for primary total knee arthroplasty based on physical exam and medical history, including diagnosis of severe knee pain and disability due to osteoarthritis, limited to:
Mild or Moderate valgus, varus, or flexion deformities
Patient must be willing and able to complete the protocol required follow-up
Patient is indicated for a 58mm or 30mm tibial stem extension
Patient has participated in the study-related informed consent process
Patient is willing and able to provide written Informed Consent by signing and dating the IRB approved informed consent
Patient has a platform-compatible personal computer located in their dwelling with appropriate wireless internet access and a USB port
Independent of study participation, patient is a candidate for commercially available Persona Personalized Knee System implanted in accordance with product labeling

Exclusion Criteria

Simultaneous bilateral TKA
Staged bilateral TKA less than 6 months from indexed procedure
Patient is a current alcohol or drug abuser
Patient is known to be pregnant, breastfeeding, or considered a member of a protected class (e.g., prisoner, mentally incompetent, etc.)
Patient has a psychiatric illness or cognitive deficit that will not allow proper informed consent and participation in follow-up program
Patient has previous history of infection in the affected joint and/or a local or systemic infection that may affect the prosthetic joint
Patient with mental or neurologic conditions who are unwilling or incapable of following postoperative care instructions
Patient with skeletal immaturity
Patient has insufficient bone stock on femoral or tibial surfaces
Patient with Neuropathic Arthropathy
Patient has osteoporosis, or any loss of musculature or neuromuscular disease that compromises the affected limb
Patient has severe instability secondary to the absence of collateral ligament integrity.
Patient has a stable, painless arthrodesis in a satisfactory functional position
Patient has 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 to one or more of the implant materials
Patient is undergoing procedures or treatments using ionizing radiation
Patients with known symptomatic foot, hip, or spinal injuries and/or conditions that could affect gait

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 Spartanburg?

Yes, this clinical trial (NCT06040827) has an active research site in Spartanburg, SC 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.

Knee Osteoarthritis Treatment Options in Spartanburg, SC

If you're searching for knee osteoarthritis treatment options in Spartanburg, SC, this clinical trial (NCT06040827) 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 Spartanburg research site is actively enrolling participants for this clinical trial. You'll receive care from experienced knee osteoarthritis 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 knee osteoarthritis clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Spartanburg, SC