Falls Church, VANCT07225751Now EnrollingIRB Ready

Ankle Arthrodesis or Arthroplasty Clinical Trial in Falls Church, VA

Access cutting-edge ankle arthrodesis or arthroplasty treatment through this clinical trial at a research site in Falls Church. Study-provided care at no cost to qualified participants.

Sponsored by Kuros Biosurgery AG

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Expert Care in Falls Church

Access ankle arthrodesis or arthroplasty specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related ankle arthrodesis or arthroplasty treatment provided free

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Check if you qualify for this ankle arthrodesis or arthroplasty clinical trial in Falls Church, VA

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Why Participate?

  • No-Cost Study Care

  • Local to Falls Church

    Convenient for VA 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 Falls Church site if eligible
  4. 4Begin participation

About This Ankle Arthrodesis or Arthroplasty Study in Falls Church

This is a phase IV post-marketing study for MagnetOs Putty and MagnetOs Easypack Putty. MagnetOs is a synthetic bone graft extender product that is routinely used by surgeon as treatment for hindfoot and ankle disorders. In this study, MagnetOs Putty and MagnetOs Easypack Putty will be use according to the latest Instructions For Use, standalone in the foot and ankle.

Sponsor: Kuros Biosurgery AG

Who Can Participate

Inclusion Criteria

Patient is able to read/be read, understand, and provide written informed consent and has signed the IRB approved informed consent.
Male or female patient ≥ 18 (considered skeletally mature) up to and including 75 years old
Patients requiring one of the following hindfoot fusion procedures, using surgical technique, necessitating rigid hardware fixation and supplemental bone graft/ substitute: ankle fusion (tibiotalar) subtalar fusion (talocalcaneal), calcaneocuboid fusion, talonavicular fusion, OR double fusion (any combination of any two of the following: subtalar, talonavicular and calcaneocuboid joints).
Hardware parameters - rigid fixation using screws, plates, staples, nails or a combination.

Exclusion Criteria

Expected to need secondary intervention within one year following surgery.
Had prior fusion or attempted fusion of the joints to be fused.
Patient is not ambulatory.
Surgical technique where bone graft is not expected to be used.
Conditions at the surgeon's discretion in which general bone grafting is not advisable.
Radiographic evidence of fractures or pathologies around the fusion that could negatively impact the fusion process (e.g., growth plate fracture around the fusion or bone cysts).
Significant vascular impairment proximal to the graft site.
Acute and/or chronic infections in the operated area (soft tissue infections; bacterial bone diseases; osteomyelitis)
Pre-existing sensory impairment (e.g. diabetes, Charcot). Diabetics patients with HbA1c greater than 7.0 OR that were not sensitive to the 5.07 monofilament will be excluded.
Metabolic disorders know to adversely affect the skeleton (e.g., renal osteodystrophy or hypercalcemia).
If intraoperative soft tissue coverage is not planned or possible.
Receiving treatment with medication interfering with calcium metabolism (chronic use of glucocorticoid and use high dose NSAIDs 800 mg TID for \> the first 6 weeks post-op).
Has benign or malignant tumor at the surgical site.
Has history or presence of active malignancy (non-invasive skin cancer is allowed).
Has known substance abuse, psychiatric disorder, or a condition which, in the opinion of the investigator, may influence the healing or ability to comply with protocol requirements (e.g. prisoners, physically or mentally compromised, etc.).
Is involved in active litigation relating to his/her foot and ankle condition.
Participation in an investigational study within 30 days prior to surgery for study devices.
Patient with body mass index (BMI) \> 50.
Patient cannot comply with all post-operative evaluation and visits .
Any pre-existing condition that the surgeon determines could interfere with the patient's ability to perform objective functional measurements.
Women who are or intend to become pregnant within the next 12 months.

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 Falls Church?

Yes, this clinical trial (NCT07225751) has an active research site in Falls Church, VA 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.

Ankle Arthrodesis or Arthroplasty Treatment Options in Falls Church, VA

If you're searching for ankle arthrodesis or arthroplasty treatment options in Falls Church, VA, this clinical trial (NCT07225751) 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 Falls Church research site is actively enrolling participants for this clinical trial. You'll receive care from experienced ankle arthrodesis or arthroplasty 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 ankle arthrodesis or arthroplasty clinical trials near you to find additional studies recruiting in your area.

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