Charleston, SCNCT05364606Now EnrollingIRB Ready

Avascular Necrosis of the Talus Clinical Trial in Charleston, SC

Access cutting-edge avascular necrosis of the talus treatment through this clinical trial at a research site in Charleston. Study-provided care at no cost to qualified participants.

Sponsored by Paragon 28

Quick Self-Assessment

See if you qualify for this Charleston location

Preparing your pre-screening questions…

Expert Care in Charleston

Access avascular necrosis of the talus specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related avascular necrosis of the talus treatment provided free

Apply for This Charleston Location

Check if you qualify for this avascular necrosis of the talus clinical trial in Charleston, SC

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Charleston

    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 Charleston site if eligible
  4. 4Begin participation

About This Avascular Necrosis of the Talus Study in Charleston

Humanitarian Device Exemption Approved Patient Specific Talus Spacer Post Approval Study.

Sponsor: Paragon 28

Who Can Participate

Inclusion Criteria

Subject plans to undergo implantation of the Patient Specific Talus Spacer for avascular necrosis of the ankle joint independent of this research protocol;
Avascular necrosis of the ankle joint;
Age 21 years old or older;
Subject has good general health; and
Subject signs a written informed consent form (ICF) prior to the surgical procedure.

Exclusion Criteria

Presence of any contraindication identified in the device Instructions for Use;
Surgeon determines that the patient is not appropriate for the Talus Spacer procedure based on the device IFU (including the enumerated Warnings and Precautions);
Based on the medical opinion of the surgeon, the patient is not appropriate for the Talus Spacer procedure;
For female subjects, pregnancy;
Active systemic disease, such as AIDS, HIV, or active infection;
Active infection or the skin is compromised at the surgical site; and
Systemic disease that would affect the subject's welfare;
Is a prisoner, incarcerated, or has been coerced to participate in the study that could impact the validity of results;
Is currently participating in an investigational therapy (device and/or pharmaceutical) within 30 days prior to entering the study or such treatment is planned during the time course of follow-up.
If the Sponsor has notified the site that 30 subjects have been enrolled in the study with a Cobalt Chromium Patient Specific Talus Spacer, and the surgeon believes that a Cobalt Chromium Patient Specific Talus Spacer is the best option for the patient.
If the Sponsor has notified the site that 30 subjects have been enrolled in the study with a Titanium (Ti6Al4V) with Titanium Nitride (TiN) coating Patient Specific Talus Spacer, and the surgeon believes that a Titanium (Ti6Al4V) with Titanium Nitride (TiN) coating Patient Specific Talus Spacer is the best option for the patient.

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 Charleston?

Yes, this clinical trial (NCT05364606) has an active research site in Charleston, 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.

Avascular Necrosis of the Talus Treatment Options in Charleston, SC

If you're searching for avascular necrosis of the talus treatment options in Charleston, SC, this clinical trial (NCT05364606) 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 Charleston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced avascular necrosis of the talus 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 avascular necrosis of the talus clinical trials near you to find additional studies recruiting in your area.

More Ankylosing Spondylitis Trials in Charleston, SC

See all ankylosing spondylitis clinical trials recruiting in Charleston — not just this study.

Browse Ankylosing Spondylitis Trials in Charleston

Ready to Join in Charleston?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Charleston, SC