Louisville, KYNCT05424354Now EnrollingIRB Ready

Wounds and Injuries Clinical Trial in Louisville, KY

Access cutting-edge wounds and injuries treatment through this clinical trial at a research site in Louisville. Study-provided care at no cost to qualified participants.

Sponsored by ULURU Inc.

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Expert Care in Louisville

Access wounds and injuries specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related wounds and injuries treatment provided free

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Check if you qualify for this wounds and injuries clinical trial in Louisville, KY

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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 Louisville

    Convenient for KY 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 Louisville site if eligible
  4. 4Begin participation

About This Wounds and Injuries Study in Louisville

This study is being performed to assess the effectiveness of Altrazeal(R) Transforming Powder Dressing (TPD) in patients with partial thickness burns compared to the current standard of care (SOC) dressing. Adult men and women 18-65 years old who are hospitalized with an acute (meaning the burn injury occurred less than 72 hours prior to enrollment in the study) partial thickness burn wound, less than 20 percent of total body surface area may be considered. Subjects will be randomized in a 1:1 ratio to either SOC or TPD. Subjects will be followed for up to 28 days after enrollment.

Sponsor: ULURU Inc.

Who Can Participate

Inclusion Criteria

Hospitalized patients who are receiving burn care; patients may be discharged when clinically stable and continue with outpatient treatment.
Men and women (women cannot be pregnant or breast feeding) ages 18-65 years old
Wounds must be partial thickness, involving up to 20% of the total body surface area.
Burn injury should be less than 72 hours old
Willing and able to comply with protocol mandated scheduled study visits/clinical evaluations.
Willing and able to provide written informed consent.

Exclusion Criteria

Known allergy to TPD or its components
Women who are pregnant, breast feeding, or plan to get pregnant during the study period.
Infected wounds
Presence of any full thickness (third degree) burns
Electrical burns
Heavily draining burns due to underlying chronic lymphedema or other conditions
Concurrent clinical condition within the judgement of the clinician, pose a health risk to the patient, delay wound healing, or otherwise influence the outcome of the study.
History of poor wound healing and/or skin/immune system condition
Deemed by clinician not to be suitable
Unwilling or not able to provide consent or comply with protocol or required visits
Developmental disability/significant psychological disorder which can impair the subjects ability to provide informed consent, or participate in the study protocol
Active alcohol or substance abuse

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 Louisville?

Yes, this clinical trial (NCT05424354) has an active research site in Louisville, KY 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.

Wounds and Injuries Treatment Options in Louisville, KY

If you're searching for wounds and injuries treatment options in Louisville, KY, this clinical trial (NCT05424354) 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 Louisville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced wounds and injuries 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.

Ready to Join in Louisville?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Louisville, KY