Marksville, LANCT06918561Now EnrollingIRB Ready

Open Wound Clinical Trial in Marksville, LA

Access cutting-edge open wound treatment through this clinical trial at a research site in Marksville. Study-provided care at no cost to qualified participants.

Sponsored by NuScience Medical Biologics, LLC

Quick Self-Assessment

See if you qualify for this Marksville location

Preparing your pre-screening questions…

Expert Care in Marksville

Access open wound specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related open wound treatment provided free

Apply for This Marksville Location

Check if you qualify for this open wound clinical trial in Marksville, LA

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Marksville

    Convenient for LA 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 Marksville site if eligible
  4. 4Begin participation

About This Open Wound Study in Marksville

This is a randomized controlled crossover trial evaluating the efficacy of NeoThelium FT in conjunction with standard of care vs. standard of care alone in treating chronic open wounds.

Sponsor: NuScience Medical Biologics, LLC

Who Can Participate

Inclusion Criteria

Male or Female, 18 years of age or older
Subject has a medical diagnosis of "other" Open wound
Subject has a chronic open wound present for 4 weeks or greater (documented in medical record), and less than 12 months duration if being treated with continuous SOC
Subject has a chronic open wound with a historical wound measurement showing less than 25% healing within 14 days prior to screening
Subject has a chronic open wound with screening wound measurement showing less than 25% healing within 14 days prior to randomization
Subject has an Open wound without infection or clinically visible exposed bone
Index wound is a minimum of 0.5cm2 and a maximum of 25cm2 at first treatment visit
Index ulcer has a maximum depth of 1cm at screening visit 1
The chronic open wound is treated with offloading therapy, if applicable to location, while standing, sitting, and lying down for 14 days prior to randomization
Adequate circulation of wounds located below the knee demonstrated by an ABI of \>0.7 and \<1.3, or TBI of \>0.6 within 30 days prior to randomization OR an arterial ultrasound noted with patent circulation and without significant stenosis 90 days prior to randomization.
Index ulcer is free of infection prior to randomization and during screening phase.
Index ulcer is free of necrotic debris prior to NeoThelium FT application
Female subjects of childbearing potential having a negative pregnancy test prior to randomization
Index ulcer is free of infection prior to randomization and during screening phase noted with the NERDS Assessment. Infection must be adequately treated and controlled prior to randomization.
Subject is able and willing to follow the protocol requirements
Subject had signed informed consent
If 2 or more ulcers are present, the ulcers must be separated by at least 2 cm

Exclusion Criteria

Subject with a wound diagnosis of diabetic foot wound, pressure wound, venous leg wound, burn wound, or alternative diagnosis other than "open wound"
Subject has a known life expectancy of \<1 year
Subject is unable to comply with protocol treatment
Subject has major uncontrolled medical disorders in the opinion of the investigator, such as serious cardiovascular, renal, liver, pulmonary, autoimmune, palliative care, or inherited blood disorders that may affect wound healing.
Subject actively being treated for malignant disease or history of malignancy or radiation therapy at the site of wound
Subject has comorbid conditions that may compromise subject safety in the opinion of the investigator
Known contraindications to tissue-engineered allograft
Concurrent participation in alternative clinical trial that involves investigational drug or product interfering with wound treatment and/or healing
Subject is pregnant or breastfeeding
Subject with history of immunosuppressant treatment (systemic corticosteroids \>10mg daily dose), cytotoxic chemotherapy, or topical steroid application to the wound surface for \>2 weeks duration within 30 days prior to randomization; or anticipated use of the above during the course of the study
Wound previously treated with CAMPs, tissue engineered, or scaffold materials within 30 days prior to randomization
Open wound with active infection
Wound depth with visible exposed bone
HBOT within 14 days prior to randomization
Revascularization surgery on the index wound leg within 30 days of screening phase
Index wound suspicious of neoplasm in the opinion of the principal investigator

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 Marksville?

Yes, this clinical trial (NCT06918561) has an active research site in Marksville, LA 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.

Open Wound Treatment Options in Marksville, LA

If you're searching for open wound treatment options in Marksville, LA, this clinical trial (NCT06918561) 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 Marksville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced open wound 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 open wound clinical trials near you to find additional studies recruiting in your area.

More Pulmonary Embolism Trials in Marksville, LA

See all pulmonary embolism clinical trials recruiting in Marksville — not just this study.

Browse Pulmonary Embolism Trials in Marksville →

Browse More Trials by Condition

Pulmonary Embolism TrialsAll Conditions →

Ready to Join in Marksville?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Marksville, LA