Clinical Utility of an Amniotic Membrane Allograft for Diabetic Foot Ulcer Wound Management (REBOUND)

Legacy Medical Consultants

Status: Not yet enrolling

Conditions: Diabetic Foot Ulcer

Treatments: Device: Orion TM Amniotic Membrane Allograft; Procedure: Standard of Care (SOC)

Study type: Interventional

Funder types: Industry

Identifiers

NCT06420245

LEGA-CLIN-2024-01

Details and patient eligibility

About

The goal of this clinical trial is to learn if use of Orion™, a dual-layer amniotic membrane allograft, in addition to standard wound care treatment can improve patient outcomes for people over the age of 50 with diabetic foot ulcers. The study aims to determine the incidence of complete wound closure at the end of 12 weeks of treatment. Researchers will compare the outcomes between a group of people treated with standard wound care and another group treated with standard wound care in addition to the amniotic membrane allograft to see if the amniotic membrane allograft improves wound healing.

During the study, participants will visit their doctor weekly over a 12 week period, which is standard for diabetic foot ulcer treatment procedures, and fill out a questionnaire measuring quality of life.

Full description

Lower extremity diabetic ulcers are a common complication affecting millions of people in the United States. The purpose of this study is to evaluate the clinical utility of Orion™, a dual-layer amniotic membrane allograft, versus standard wound care in the management of diabetic foot ulcers. Amniotic membrane allografts are confirmed by the FDA Tissue Reference Group to meet the criteria for regulation solely under Section 361 of the PHS Act as defined in 21 CFR Part 1271 for the management of diabetic foot ulcers. Investigators hypothesize that the group of participants who receive amniotic membrane allografts in addition to standard wound care will experience a faster rate and higher incidence of complete wound closure compared to standard wound care alone. For only partially healed wounds, investigators anticipate a statistically significant reduction in the size of the ulcer and improved quality of life for participants in the experimental arm compared to standard wound care alone.

Enrollment: 240 estimated patients

Sex: All

Ages: 50 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

1. Ambulatory patients ≥ 50 and ≤ 85 years of age;
2. Willing and able to provide informed consent;
3. Willing and able to comply with study requirements;
4. Presence of Wagner 1 and superficial Wagner 2 DFU extending at least through the dermis provided the DFU is located in the foot distal to the medial malleolus
5. If multiple Wagner 1 and superficial Wagner 2 DFUs are present, the largest ulcer meeting DFU eligibility criteria will be selected as the index DFU in the study;
6. Index ulcer is able to be visualized and accurately measured with eKare Insights;
7. Non-study ulcers must be > 2 cm (.79 in.) from the index ulcer;
8. Index DFU identified ≥ 4 weeks prior to study screening and < 52 weeks from the date of informed consent;
9. Index DFU area > 1.0 cm2 (0.39 in.) and < 25 cm2 (9.84 in.) at screening and at Wound Management Period Visit #1;
10. Index DFU offloaded according to SOC for entire run-in period, prior to randomization;
11. Potential participant is under the care of a clinician for diabetic management and other medical conditions (the site PI may assist/direct the patient in the pre-screening period to obtain a PCP).
12. Index foot has adequate circulation defined as meeting one (1) of the following within 30 days of screening:

A. ABI ≥ 0.7 and ≤ 1.3 AND TBI > 0.7; B. Dorsum transcutaneous oxygen tension measurement (TcPO2) ≥ 40 mmHg; C. Arterial duplex with biphasic flow in BOTH the DP and PT arteries verified by PI and documented.

Exclusion Criteria

1. Index foot ulcer documented to be caused by a medical condition other than diabetes;

2. Potential subject has five (5) or more DFUs and/or VLUs in the target limb;

3. DFU is secondary to Charcot neuroarthropathy;

4. Treatment with an antibiotic impregnated primary dressing ≤ 4 weeks prior to study screening;

5. Index ulcer is potentially or confirmed by biopsy to be cancerous;

6. Index ulcer site has undergone radiation therapy;

7. Venous leg ulcers in diabetic patients;

8. Active infection proximal to or at site of index ulcer;

9. Index foot ulcer reduced in area by ≥ 20% at the end of the 4-week run-in period;

10. Presence of active osteomyelitis or bone infection as verified by x-ray /MRI within 30 days of visit #1 of the run-in period;

11. Raynaud's disease;

12. Unreconstructible arterial ischemia which may lead to nonhealing;

13. Treatment with immunosuppressants, including systemic corticosteroids for ≥ 2 weeks within 30 days prior to study screening, or are anticipated during study participation;

14. Any active cancer undergoing treatment ≤ 30 days prior to wound management visit #1 of the run-in period, or is anticipated during study participation;

15. Treatment with chemotherapy within 30 days of the first study wound management visit of the run-in period, or is anticipated during study participation;

16. Diabetics with poor metabolic control, defined as HbA1c ≥ 12.0%, within 30 days of visit #1 of the run-in period;

17. Participation in an investigational device, biologic, or drug study currently or within 30 days of study wound management visit #1 of the run-in period;

18. Prior use of any advanced skin substitute product on the index ulcer within 60 days of visit #1 of the run-in period;

19. Index ulcer was continued to be treated after visit #1 of the run-in period and/or anticipate treatment during study participation with any of the following prohibited therapies:

    1. Biomedical or topical growth factor;
    2. Topical steroids applied to the index ulcer surface;
    3. On medications that are considered immune system modulators that could affect graft incorporation;
    4. Scarlet red dressing;
    5. Dakin's solution;
    6. Mafenide acetate;
    7. Tincoban;
    8. Zinc sulfate;
    9. Povidone-iodine solution;
    10. Polymyxin/nystatin;
    11. Chlorhexidine;

20. Patient is taking a cyclooxygenase-2 inhibitor (COX-2 inhibitor); such as, celecoxib (Celebrex, Consensi, Elyxyb), valdecoxib (Bextra), amlodipine (Consensi);

21. Patient has serum creatinine > 2.5 mg/dL within 30 days of study wound management visit #1 of the run-in period;

22. Autoimmune connective tissue disease;

23. End stage renal disease (ESRD);

24. Presence of any condition which would seriously compromise the subject's ability to complete this study;

25. Known history of poor adherence to medical therapy and/or clinic appointments;

26. Pregnant, or planning to become pregnant during the study;

27. Life expectancy < 1 year.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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240 participants in 2 patient groups

Standard of Care (SOC)

Active Comparator group

Description:

Standard of care DFU wound management

Treatment:

Procedure: Standard of Care (SOC)

Amniotic Membrane plus Standard of Care

Experimental group

Description:

Weekly application of Orion™ amniotic membrane allograft in addition to standard of care DFU wound management

Treatment:

Procedure: Standard of Care (SOC)

Device: Orion TM Amniotic Membrane Allograft