The Bronx, NYNCT05206981Now EnrollingIRB Ready

Traumatic Fracture Clinical Trial in The Bronx, NY

Access cutting-edge traumatic fracture treatment through this clinical trial at a research site in The Bronx. Study-provided care at no cost to qualified participants.

Sponsored by IlluminOss Medical, Inc.

Quick Self-Assessment

See if you qualify for this The Bronx location

Preparing your pre-screening questions…

Expert Care in The Bronx

Access traumatic fracture specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related traumatic fracture treatment provided free

Apply for This The Bronx Location

Check if you qualify for this traumatic fracture clinical trial in The Bronx, NY

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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 The Bronx

    Convenient for NY 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 The Bronx site if eligible
  4. 4Begin participation

About This Traumatic Fracture Study in The Bronx

This is a multi-center, observational patient registry. The primary objective of the study is to collect safety and performance data on the IlluminOss Device when used to provide stabilization and alignment for the treatment of traumatic or impending and pathologic fractures.

Sponsor: IlluminOss Medical, Inc.

Who Can Participate

Inclusion Criteria

Patient has been deemed a candidate for the IlluminOss device
Patient is male or non-pregnant female
Patient is willing and able to comply with the postoperative scheduled clinical and radiographic evaluations
Patient is willing and able to give informed consent if required
Traumatic patient is over the age of 50
IlluminOss procedure is the initial procedure to treat the traumatic injury

Exclusion Criteria

United States (U.S.) This product is contraindicated in U.S. patients who have:
an active or incompletely treated infection that could involve the site where the device will be implanted;
are allergic to any of the implant materials or to dental glue;
have an intramedullary canal measuring smaller than the diameter of the delivery sheath provided at the site of the fracture;
distant foci of infections which may spread to the implant site, have open fractures with severe contamination;
or in patients for whom delivery sheath is unable to cross fracture site after proper fracture reduction and realignment. European Union (EU) This product is contraindicated in EU patients who have: For all Bones:
Patients who are considered skeletally immature.
Presence of active or incompletely treated infections that could involve the site where the device will be implanted.
Patients allergic to any of the implant materials, or to dental glue.
Patients whose intramedullary canal at site of fracture measures smaller than the diameter of the sheath provided.
Uncooperative patient or patient with neurologic disorder, incapable of following directions.
Distant foci of infections which may spread to the implant site.
Vascular insufficiency.
Open fractures with severe contamination.
Extremely comminuted fractures where insufficient holding power of the balloon on the intramedullary canal is probable.
Delivery sheath is unable to cross fracture site after proper fracture reduction and realignment. For acute Humerus fractures:
Patients who are under the age of Fifty (50) For all bones excluding pathologic Humerus:
Metabolic disorders which may impair bone formation.
Osteomalacia.
Vascular insufficiency, muscular atrophy, or neuro-muscular disease.

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 The Bronx?

Yes, this clinical trial (NCT05206981) has an active research site in The Bronx, NY 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.

Traumatic Fracture Treatment Options in The Bronx, NY

If you're searching for traumatic fracture treatment options in The Bronx, NY, this clinical trial (NCT05206981) 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 The Bronx research site is actively enrolling participants for this clinical trial. You'll receive care from experienced traumatic fracture 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 traumatic fracture clinical trials near you to find additional studies recruiting in your area.

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