Lansdowne, VANCT05883241Now EnrollingIRB Ready

Bone Fracture Clinical Trial in Lansdowne, VA

Access cutting-edge bone fracture treatment through this phase 1 clinical trial at a research site in Lansdowne. Study-provided care at no cost to qualified participants.

Sponsored by ZetrOZ, Inc.

Quick Self-Assessment

See if you qualify for this Lansdowne location

Preparing your pre-screening questions…

Expert Care in Lansdowne

Access bone fracture specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related bone fracture treatment provided free

Apply for This Lansdowne Location

Check if you qualify for this bone fracture clinical trial in Lansdowne, VA

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Lansdowne

    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 Lansdowne site if eligible
  4. 4Begin participation

About This Bone Fracture Study in Lansdowne

The purpose of this study is to assess the ability of long-duration low-intensity therapeutic ultrasound (LITUS) to alleviate bone-fracture related pain over a 12-week period. The primary objective of this study is to evaluate the analgesic effect of LITUS in subjects suffering from bone-fracture pain. Secondary objectives are to assess the ability of LITUS to improve patients return to work time.

Sponsor: ZetrOZ, Inc.

Who Can Participate

Inclusion Criteria

Have physician-diagnosed bone fracture
Are between 18-80 years of age
Report a pain score between 3-7 (range: 0-10) prior to enrolment
Report that pain from fracture negatively affects quality of life
Are willing not to use any cream, gel, or topical solution during the administration of treatment other than the approved treatment provided to the subject at the initiation of the study
Are deemed appropriate by their physician or by the study site physician to participate.
Be willing and able to self-administer treatment daily within their place of residence or during normal daily activity, excluding bathing, showering, or other water activities which may result in submersion of the study device.
Not use or initiate opioid and/or non-opioid analgesic medications.
Be willing to discontinue any other interventional treatment modalities on the affected area during the study period (e.g., transcutaneous electrical nerve stimulation, electronic muscle stimulation, traditional ultrasound).

Exclusion Criteria

Cannot successfully demonstrate the ability to put on and take off the device.
Displays any condition which, in the judgment of the investigator, would make participation in the study unacceptable including, but not limited to, the subject's ability to understand and follow instructions.
Participated in a clinical trial for an investigational drug and/or agent within 30 days prior to screening.
Is pregnant.
Is a prisoner.
Is non-ambulatory (unable to walk).
Has a pacemaker.
Has a malignancy in the treatment area.
Has an active infection, open sores, or wounds in the treatment area.
Has impaired sensation in the treatment area, such as caused by chemotherapy or anesthesia.
Has a known neuropathy (disease of the brain or spinal nerves).
Has a hereditary disposition (tendency) for excessive bleeding (hemorrhage).
Are currently taking steroids.

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 Lansdowne?

Yes, this clinical trial (NCT05883241) has an active research site in Lansdowne, 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.

Bone Fracture Treatment Options in Lansdowne, VA

If you're searching for bone fracture treatment options in Lansdowne, VA, this clinical trial (NCT05883241) 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 Lansdowne research site is actively enrolling participants for this phase 1 clinical trial. You'll receive care from experienced bone 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 bone fracture clinical trials near you to find additional studies recruiting in your area.

More Rheumatoid Arthritis Trials in Lansdowne, VA

See all rheumatoid arthritis clinical trials recruiting in Lansdowne — not just this study.

Browse Rheumatoid Arthritis Trials in Lansdowne →

Browse More Trials by Condition

Rheumatoid Arthritis TrialsAll Conditions →

Ready to Join in Lansdowne?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Lansdowne, VA