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Study identifier: NCT07116876 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Matrion Decellularized Placental Membrane Versus Conventional Wound Management in Subjects With Diabetic Foot Ulcers

Condition: Diabetic Foot Ulcer (DFU) · Lower Extremity  ·  Sponsor: LifeNet Health

PhaseNA
Planned participants120
Who can joinAll sexes, 21 Years to 80 Years
Healthy volunteersNo

About this study

This study will evaluate Matrion™ (LifeNet Health, Inc., Virginia Beach, VA), a placental membrane product, as a treatment for diabetic foot ulcers compared to conventional wound care. Matrion is derived from donated human birth tissue and includes both the amniotic and chorionic layers, along with the trophoblast layer. It is minimally processed using a proprietary decellularization method and terminally sterilized to ensure the membrane is acellular and sterile, making it suitable for surgical applications.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

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Locations (18)

Compass Medical Research CenterTucson, Arizona, United StatesRecruiting
Bay Area Foot CareCastro Valley, California, United StatesRecruiting
Limb Preservaion Platform, Inc.Fresno, California, United StatesRecruiting
Center for Clinical Research, IncSan Francisco, California, United StatesRecruiting
Bay Area Foot CareSan Francisco, California, United StatesRecruiting
ILD Research CenterVista, California, United StatesRecruiting
Humanity Clinical Research, CorpAventura, Florida, United StatesRecruiting
South Florida PodiatryDeerfield Beach, Florida, United StatesRecruiting
Dinamo Research & Diagnostic Center, LLCHialeah, Florida, United StatesRecruiting
Doctors Research Network, Inc.Miami, Florida, United StatesRecruiting
Independent Clinical ResearchDecatur, Illinois, United StatesRecruiting
Independent Clinical Research, LLCSpringfield, Illinois, United StatesRecruiting

+ 6 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07116876