Cincinnati, OHNCT07244211Now EnrollingIRB Ready

Femoral Neck Fractures Clinical Trial in Cincinnati, OH

Access cutting-edge femoral neck fractures treatment through this clinical trial at a research site in Cincinnati. Study-provided care at no cost to qualified participants.

Sponsored by University of Southern California

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Expert Care in Cincinnati

Access femoral neck fractures specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related femoral neck fractures treatment provided free

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Check if you qualify for this femoral neck fractures clinical trial in Cincinnati, OH

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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 Cincinnati

    Convenient for OH 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 Cincinnati site if eligible
  4. 4Begin participation

About This Femoral Neck Fractures Study in Cincinnati

This study is an intervention domain of the Musculoskeletal Adaptive Platform Trial. The primary goal of this pragmatic, randomized, open-label, comparative effectiveness trial is to evaluate if arthroplasty is superior to internal fixation when used to treat minimally displaced femoral neck fractures in older adults ≥60 years old. We hypothesize that arthroplasty will reduce death, preserve ambulation, increase days alive and out of hospital, and improve health status compared to internal fixation within 4 months and 12 months from randomization.

Sponsor: University of Southern California

Who Can Participate

Inclusion Criteria

60 years of age or older undergoing surgery due to a minimally displaced femoral neck fracture
The patient has a health condition affecting physical mobility.
Complete fracture of the femoral neck (AO/OTA 31B) confirmed with anteroposterior and lateral hip radiographs, computed tomography, or magnetic resonance imaging.
Minimally displaced fracture that could be, in the judgment of the attending surgeon, managed with either arthroplasty or in situ internal fixation without reduction.
Low energy injury mechanism.
Surgeons with expertise in internal fixation and total hip arthroplasty or hemiarthroplasty are available to perform surgery.

Exclusion Criteria

The patient is not clinically suitable for either compared treatment.
Expected injury survival of less than 12 months.
Terminal illness with expected survival of less than 12 months.
Incarceration.
Unable to obtain informed consent due to language barriers.
Unable to obtain informed consent because the legally authorized representative was unavailable.
Problems, in the judgment of the study personnel, with maintaining follow-up with the patient.
Currently enrolled in a study or intervention domain that does not permit co-enrollment.
Prior enrollment in the specific platform trial intervention domain.
Patient or legally authorized representative did not provide informed consent (declined participation).
Eligible patient or legally authorized representative was not approached within the screening window (missed participant).
Other reasons to exclude the patient, as approved by the data coordinating center.
Associated lower extremity injury that prevents post-operative weight-bearing.
Retained hardware around the hip that precludes either study treatment.
Infection around the hip (soft tissue or bone).
Pathologic fracture with a lytic lesion in the femoral neck that precludes internal fixation.
Injury did not occur within 21 days of screening.
Patient is too ill, in the judgment of the attending surgeon, for internal fixation.
Patient is too ill, in the judgment of the attending surgeon, for arthroplasty.

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 Cincinnati?

Yes, this clinical trial (NCT07244211) has an active research site in Cincinnati, OH 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.

Femoral Neck Fractures Treatment Options in Cincinnati, OH

If you're searching for femoral neck fractures treatment options in Cincinnati, OH, this clinical trial (NCT07244211) 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 Cincinnati research site is actively enrolling participants for this clinical trial. You'll receive care from experienced femoral neck fractures 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 femoral neck fractures clinical trials near you to find additional studies recruiting in your area.

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