Clinical trials

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Condition / disease
Location
Status: Recruiting

Non-healing Venous Leg Ulcers Treated With Standard Care With or Without BR-AC

This study examines a patient population with a non-healing, non-infected venous leg ulcer (VLU) having adequate arterial perfusion with confirmed venous reflux. It is hypothesized that weekly applications of the human placental allograft BioREtain® Amnion Chorion (BR-AC) applied to a non-healing VLU will result in a higher proportion of wounds showing complete healing within 12 weeks of initiating therapy, compared to standard care alone. This study has a crossover period, where subjects on standard care alone who do not achieve complete healing within 12 weeks of initiating therapy will be allowed to crossover to receive BR-AC over 12 additional weeks, to evaluate if their wound can achieve complete healing.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: BioStem TechnologiesUpdated: Jan 23, 2026Locations: 23
Eligibility criteria

Patient has signed the informed consent form. [+11]

A target ulcer of non-venous etiologies (e.g., sickle cell anemia, necrobiosis l... [+18]