Evaluating the Efficacy of OCM™ (Omeza® Complete Matrix) in the Treatment of Diabetic Foot Ulcers

Recruiting now · Not applicable

Conditions studied: Diabetic Foot Ulcer

In brief

This study aims to compare two treatment approaches for diabetic foot ulcers (DFUs): the standard of care (SOC) alone versus SOC combined with OCM. Researchers will evaluate whether adding OCM increases the likelihood of ulcers healing completely by the end of the trial period.

Key facts

Study ID

NCT07161830

Run by

Omeza, LLC

People needed

180

Starts

2025-12-04

Expected to finish

2027-03-30

Last updated by the study team

2026-08-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or Female, 18 years of age or older
• Subject has a medical diagnosis of Type I or Type II Diabetes Mellitus requiring oral or glycemic control and/or insulin replacement therapy
• Subject has a diabetic foot ulcer present for 4 weeks or greater (documented in medical record) and being treated with continuous SOC
• Subject has a diabetic foot ulcer with a historical wound measurement showing less than 25% healing in 14 days prior to screening
• Subject has a diabetic foot ulcer with screening wound measurement showing less than 25% healing in 14 days prior to randomization
• Subject has a diabetic foot ulcer of Wagner grade 1 or 2
• Index ulcer is a minimum of 0.7cm2 and a maximum of 25cm2 at first treatment visit
• Diabetic foot ulcer is being treated with offloading therapy for 14 days prior to randomization
• Adequate circulation of ulcer 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. Infection must be adequately treated and controlled as defined by Infectious Disease Society of America (IDSA) Guidelines PEDIS Grade 1.
• Index ulcer is free of necrotic debris prior to OCMTM application
• Female subjects of childbearing potential having a negative pregnancy test 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

You may not qualify if…

• Subject has a known life expectance 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 fish products or cod liver oil.
• Concurrent participation in alternative clinical trial that involves investigational drug or device 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 ulcer 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 14 days prior to randomization
• Wound depth with visible exposed bone
• HBOT within 14 days prior to randomization
• Revascularization surgery on the index ulcer leg within 30 days of screening phase
• Index ulcer suspicious of neoplasm in the opinion of the principal investigator

Where it is running

• SitePath Research — Evergreen Park, Illinois, United States (enrolling)
• MedCentris of Denham Springs — Denham Springs, Louisiana, United States (enrolling)
• MedCentris of Leesville — Leesville, Louisiana, United States (enrolling)
• MedCentris of Marksville — Marksville, Louisiana, United States (enrolling)
• MedCentris of Slidell — Slidell, Louisiana, United States (enrolling)
• MedCentris of Vidalia — Vidalia, Louisiana, United States (enrolling)
• MedCentris of Cleveland — Cleveland, Mississippi, United States (enrolling)
• MedCentris of Southaven — Southaven, Mississippi, United States (enrolling)
• Gentle Foot Care — Newark, Ohio, United States (enrolling)
• Gentle Foot Care — Sylvania, Ohio, United States (enrolling)

Full record on ClinicalTrials.gov

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