Thermal Burn clinical trials at University of California Health

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  • Evaluation of the Effectiveness of PermeaDerm® (PD) as Compared to Mepilex Ag®

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    A total of 68 adult and pediatric patients who suffer from at least one discrete partial thickness thermal burn wound (Grade II) will be recruited. Subjects will be randomized (1:1) to either PermeaDerm® or Mepilex Ag®. Evaluations will occur at 7, 14 and 21 days with long term follow-up at 6 and 12 months.

    at UC Davis

Our lead scientists for Thermal Burn research studies include .

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