Tulsa, OKNCT06515093Now EnrollingIRB Ready

Diabetic Foot Ulcer Clinical Trial in Tulsa, OK

Access cutting-edge diabetic foot ulcer treatment through this clinical trial at a research site in Tulsa. Study-provided care at no cost to qualified participants.

Sponsored by Surgenex

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Expert Care in Tulsa

Access diabetic foot ulcer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related diabetic foot ulcer treatment provided free

Apply for This Tulsa Location

Check if you qualify for this diabetic foot ulcer clinical trial in Tulsa, OK

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Tulsa

    Convenient for OK 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 Tulsa site if eligible
  4. 4Begin participation

About This Diabetic Foot Ulcer Study in Tulsa

The purpose of this study is to compare Pellograft to standard of care modalities in treating diabetic foot ulcers in human subjects, and to compare Sanograft to standard of care in treating venous leg ulcers. The study will demonstrate wound healing outcomes with comparators including time to wound epithelialization, decrease in wound size, and total number of study product applications towards healing outcome. This information is important to the Centers for Medicare and Medicaid Services (CMS) and other payors in determining coverage policy and reimbursement for this product category.

Sponsor: Surgenex

Who Can Participate

Inclusion Criteria

Subject is at least 18 years of age
Diabetic Foot Ulcer Only - Subject has diagnosed Type 1 or Type 2 diabetes
Subject's wound is located on foot or ankle (DFU) or leg (VLU)
Subject has diabetic foot ulcer \> 1.0 cm2 and ≤ 25 cm2 OR venous leg ulcer \> 1.0 cm2 and ≤ 50 cm2
Subject has adequate circulation to affected extremity with TcPO2 results of ≥ 40 mm Hg on the dorsum of the affected foot or ABI results ≥ 0.7 and≤ 1.2 or Great Toe Pressure ≥ 50 mmHg
Subject is willing and able to comply with all protocol requirements
Subject is willing and able to provide informed consent or obtain consent from legal authorized representative (LAR)

Exclusion Criteria

Subject is pregnant
Subject with diagnosed diabetes has HbA1C \> 12 within 3 months Prior to randomization
Subject has \> 30% reduction in wound size after 2-week run-in period
Subject has active infection, undrained abscess, or critical colonization of the wound with bacteria
Subject has osteomyelitis or joint capsule on investigator's exam or radiographic evidence or bone culture, histology, x-ray changes or MRI
Subject is on parenteral corticosteroids or any cytotoxic agents for 7 consecutive days during 30 days before screening. Chronic oral steroid use is not excluded if dose \< 10 mg per day of prednisone
Subject is currently undergoing cancer treatment
Subject has used biologic skin substitutes within 14 days of enrollment
Subject has an allergy to suture material
Subject has life expectancy less than six-months as assessed by the investigator
Subject is participating in another clinical research study prior to this study completion

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 Tulsa?

Yes, this clinical trial (NCT06515093) has an active research site in Tulsa, OK 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.

Diabetic Foot Ulcer Treatment Options in Tulsa, OK

If you're searching for diabetic foot ulcer treatment options in Tulsa, OK, this clinical trial (NCT06515093) 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 Tulsa research site is actively enrolling participants for this clinical trial. You'll receive care from experienced diabetic foot ulcer 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 diabetic foot ulcer clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Tulsa, OK