Indianapolis, INNCT06496867Now EnrollingIRB Ready

Multiple Closed Pelvic Fractures With Disruption of Pelvic Ring Clinical Trial in Indianapolis, IN

Access cutting-edge multiple closed pelvic fractures with disruption of pelvic ring treatment through this clinical trial at a research site in Indianapolis. Study-provided care at no cost to qualified participants.

Sponsored by University of Southern California

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Expert Care in Indianapolis

Access multiple closed pelvic fractures with disruption of pelvic ring specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related multiple closed pelvic fractures with disruption of pelvic ring treatment provided free

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Why Participate?

  • No-Cost Study Care

  • Local to Indianapolis

    Convenient for IN 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 Indianapolis site if eligible
  4. 4Begin participation

About This Multiple Closed Pelvic Fractures With Disruption of Pelvic Ring Study in Indianapolis

The goal of this randomized pilot study is to assess feasibility of the trial and to collect information to inform the design of a definitive trial. Adult patients ages 60 years or older with a low-energy lateral compression type 1 (LC1) pelvis fracture with \<10 mm initial displacement of the posterior pelvic ring will be eligible to participate in the study. Patients will be randomized to one of two treatment groups, early internal fixation or nonoperative care with early rehabilitation, defined as at least five days of attempted mobilization by rehabilitation providers. Participants will be followed for 1 year.

Sponsor: University of Southern California

Who Can Participate

Inclusion Criteria

Patient 60 years of age or older.
Low energy injury mechanism defined as a fall from standing height.
LC1 pelvis fracture (AO/OTA 61B1.1 or 61B2.1) confirmed with antero-posterior, inlet, and outlet pelvis radiographs, computed tomography, or magnetic resonance imaging.
Fracture pattern that could be, in the judgment of the attending surgeon, managed with either early internal fixation or nonoperative care with early rehabilitation.
Fracture displacement of \<10 mm of the posterior pelvic ring on computed tomography of the pelvis.
Injury occurred within 21 days of screening.

Exclusion Criteria

Patient did not ambulate prior to injury.
Patient has another condition, injury, or fracture that prevents post-operative weightbearing on any extremity.
Retained implants around the pelvis that precludes or limits either study treatment.
Infection around the hip (soft tissue or bone).
Pathologic fracture with a lytic lesion in the pelvis or sacrum that precludes internal fixation.
Patient is too ill, in the judgement of the attending surgeon, for internal fixation.
Patient is too ill, in the judgement of the attending surgeon, for nonoperative care.
Problems, in the judgment of study personnel, with maintaining follow-up with the patient.
Expected injury survival of less than 12 months.
Terminal illness with expected survival of less than 12 months.
Currently enrolled in a study that does not permit co-enrollment.
Prior enrollment in the trial.
Unable to obtain informed consent due to language barriers.
Unable to obtain informed consent because a legally authorized representative (LAR) was unavailable.
Did not provide informed consent (declined participation).
Patient or LAR not approached to participate in the trial (missed patient).
Other reason to exclude the patient, as approved by the Methods Centre.

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 Indianapolis?

Yes, this clinical trial (NCT06496867) has an active research site in Indianapolis, IN 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.

Multiple Closed Pelvic Fractures With Disruption of Pelvic Ring Treatment Options in Indianapolis, IN

If you're searching for multiple closed pelvic fractures with disruption of pelvic ring treatment options in Indianapolis, IN, this clinical trial (NCT06496867) 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 Indianapolis research site is actively enrolling participants for this clinical trial. You'll receive care from experienced multiple closed pelvic fractures with disruption of pelvic ring 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 multiple closed pelvic fractures with disruption of pelvic ring clinical trials near you to find additional studies recruiting in your area.

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