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After the peeling, participants will return within 3 weeks for 4 visits to the study center to investigate the skin conditions such redness, irritation, softness and possible side effects. In addition, study participants will be asked about their general acceptance of dexpanthenol dermal spray.
The primary objective is to evaluate the efficacy of the test product to aid skin recovery after peeling in the female intima and inguinal region.
Secondary objectives comprise clinical efficacy with respect to skin hydration, softness, vitality, appearance etc. and skin recovery, consumer judgement of product performance and acceptability, and safety.
BAY207543 (Bepanthol, Bepantol® Derma Spray), Semisolid vaseline
Medcin Instituto da Pele
Published on BioPortfolio: 2019-03-01T01:15:31-0500
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