Status:
RECRUITING
Clinical Study Evaluating Symphony™ Versus Standard of Care in the Treatment of Non-Healing Diabetic Foot Ulcers
Lead Sponsor:
Aroa Biosurgery Limited
Collaborating Sponsors:
Professional Education and Research Institute
Conditions:
Diabetic Foot
Diabetic Foot Ulcer
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The study will evaluate the safety and performance of Symphony™ versus Standard of Care (SOC) in the treatment of chronic non-healing diabetic foot ulcers (DFU) after 12 weeks of treatment.
Detailed Description
About 120 subjects will take part in this study. Subjects with a Wagner Grade 1 or 2 Diabetic Foot Ulcers will be randomized at a ratio of 1:1 to one of the two treatment groups at the time of complet...
Eligibility Criteria
Inclusion
- 1\. At least 18 years old, inclusive.
- 2\. Presence of a DFU, Wagner Grade 1 or 2 (see Appendix B for definitions), extending through the dermis provided it is below the medial aspect of the malleolus.
- 3\. The index ulcer (ulcer to be evaluated in the study) will be the largest ulcer if two or more DFUs are present with the same Wagner grade and will be the only one evaluated in the study. If other ulcerations are present on the same foot, they must be more than 2 cm distant from the index ulcer.
- 4\. Index ulcer has been present for greater than 4 weeks prior to SV1 and less than 1 year, as of the date the subject consents for study.
- 5\. Index ulcer is a minimum of 1.0 cm2 and a maximum of 25 cm2 at SV1 and TV1.
- 6\. Within 3 months of SV1, adequate circulation to the affected foot as documented by a dorsal transcutaneous oxygen measurement (TCOM) or a skin perfusion pressure (SPP) measurement of ≥ 30 mmHg, or an Ankle Branchial Index (ABI) between 0.7 and 1.3 using the affected study extremity. As an alternative, arterial Doppler ultrasound can be performed evaluating for biphasic dorsalis pedis and posterior tibial vessels at the level of the ankle or a TBI (Toe Brachial Index) of \> 0.6 is acceptable.
- 7\. The target ulcer has been offloaded for at least 14 days, prior to TV1.
- 8\. Females of childbearing potential must be willing to use acceptable methods of contraception (birth control pills, barriers or abstinence) during the course of the study and undergo pregnancy tests.
- 9\. Subject understands and is willing to participate in the clinical study and can comply with weekly visits.
- 10\. Subjects must have read and signed the IRB approved ICF before screening procedures are performed.
Exclusion
- 1\. Index ulcer(s) deemed by the investigator to be caused by a medical condition other than diabetes
- 2\. Index ulcer, in the opinion of the investigator, is suspicious for cancer and should undergo an ulcer biopsy to rule out a carcinoma of the ulcer
- 3\. Index ulcer is overtly infected (i.e., purulent drainage)
- 4\. Subjects with a history of more than two weeks of treatment with immune-suppressants (including systemic corticosteroids \>10mg daily dose), cytotoxic chemotherapy, or application of topical steroids to the ulcer surface within 1-month prior to first SV1, or who receive such medications during the screening period or who are anticipated to require such medications during the course of the study
- 5\. Subjects on any investigational drug(s) or therapeutic device(s) within 30 days preceding SV1
- 6\. History of radiation at the ulcer site (regardless of time since last radiation treatment)
- 7\. Index ulcer has been previously treated or will need to be treated with any prohibited therapies
- 8\. Subjects with a previous diagnosis of HIV or Hepatitis C
- 9\. Presence of any condition(s) which seriously compromises the subject's ability to complete this study or has a known history of poor adherence with medical treatment
- 10\. Osteomyelitis or bone infection of the affected foot as verified by xray within 30 days prior to the first screening visit. (In the event of an ambiguous diagnosis, the Principal Investigator will make the final decision)
- 11\. Subject is pregnant or breast-feeding
- 12\. Presence of diabetes with poor metabolic control as documented with an HbA1c \>12.0 within last 90 days
- 13\. Subjects with end stage renal disease as evidenced by a serum creatinine ≥3.0 mg/dL within 6 months of enrollment
- 14\. Presence of acute Charcot Neuroarthropathy to the affected limb
- 15\. Index ulcer that has reduced in area by 30% or more after 14 days of SOC from SV1 to the TV1/Randomization visit
Key Trial Info
Start Date :
June 8 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 27 2025
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT06035536
Start Date
June 8 2023
End Date
December 27 2025
Last Update
July 3 2025
Active Locations (11)
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1
LA Foot and Ankle
Los Angeles, California, United States, 90010
2
Clemente Clinical Research Inc.
Los Angeles, California, United States, 90033
3
Bay Area Foot Care
San Francisco, California, United States, 94115
4
Doctor's Research Network
Miami, Florida, United States, 33143