Evaluation of the Efficacy of Hyalomatrix® in the Healing of Chronic Venous Leg Ulcers

This is a randomized controlled trial evaluating the efficacy of HYALOMATRIX in conjunction with standard of care vs. standard of care alone in treating venous leg ulcers.

Inclusion Criteria: 1. Male or Female, 18 years of age or older 2. Subject has a medical diagnosis of venous leg ulcer or venous insufficiency with a lower extremity wound 3. Subject has a venous leg ulcer present for 4 weeks or greater (documented in medical record), and less than 12 months duration if being treated with continuous SOC 4. Subject has a venous leg ulcer with a historical wound measurement showing less than 25% healing within 14 days prior to screening 5. Subject has a venous leg ulcer with screening wound measurement showing less than 25% healing within 14 days prior to randomization 6. Subject has a venous leg ulcer without infection or clinically visible exposed bone 7. Index wound is a minimum of 1 cm2 and a maximum of 30 cm2 at first treatment visit 8. Adequate circulation if wound is location on the lower extremity demonstrated by an ABI of \>0.7 and \0.6 within 30 days prior to informed consent OR an arterial ultrasound noted with patent circulation and without significant stenosis 90 days prior to the first treatment visit. 9. Venous Leg Ulcer is being treated with compression therapy for 14 days prior to treatment visit 1 10. Index wound is free of necrotic debris prior to Hyalomatrix application 11. Female subjects of childbearing potential having a negative pregnancy test prior to randomization 12. Index wound is free of infection prior to randomization and during screening phase noted with the NERDS Assessment. Infection must be adequately treated and controlled prior to randomization. 13. Subject is able and willing to follow the protocol requirements 14. Subject had signed informed consent 15. If 2 or more wounds are present, the wounds must be separated by at least 2 cm Exclusion Criteria: 1. Subject does not have a diagnosis of venous leg ulcer or venous insufficiency with a wound located on the lower extremity 2. Subject has a known life expectancy of \10mg daily dose), cytotoxic chemotherapy, or topical steroid application to the wound surface for \>2 weeks duration within 30 days prior to randomization; or anticipated use of the above during the course of the study 11. Wound previously treated with CAMPs, tissue engineered, or scaffold materials within 30 days prior to randomization 12. Venous leg ulcer with active infection 13. Wound depth with visible exposed bone 14. HBOT within 14 days prior to randomization 15. Revascularization surgery on the index wound leg within 30 days of screening phase 16. Index wound suspicious of neoplasm in the opinion of the principal investigator