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

Launched by LEGACY MEDICAL CONSULTANTS · May 14, 2024

Keywords

ClinConnect Summary

This clinical trial is looking to see if a special treatment called Orion™, which is made from amniotic membrane (the tissue that surrounds a baby in the womb), can help heal diabetic foot ulcers better than standard wound care alone. The study involves patients who are 50 years or older and have certain types of diabetic foot ulcers. Researchers will compare two groups: one group will receive regular wound care, while the other group will receive both regular care and the Orion™ treatment. The main goal is to find out how many patients’ wounds completely heal after 12 weeks of treatment.

Participants in the study will need to visit their doctor weekly for 12 weeks and will fill out a questionnaire about their quality of life. To be eligible, participants should be ambulatory (able to walk), have a specific type of foot ulcer, and be under the care of a healthcare provider for their diabetes. However, some people may not qualify if they have other health issues, like an active infection or certain types of ulcers caused by non-diabetes-related conditions. Overall, this trial aims to provide new insights into improving healing for diabetic foot ulcers in older adults.

Gender

ALL

Eligibility 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.