Erythema Clinical Trial
Official title:
Evaluation of the Safety and Efficacy of the Product Bepantol® Derma Spray After the Dermatological Procedure in the Face - 21 Days of Follow-up.
In this study, researchers want to learn more about the effect of dexpanthenol dermal spray
on skin recovery and reduction of skin redness after a dermatological procedure (non-ablative
laser) on the face for treatment of fine wrinkles, scars, open pores and change of
pigmentation.
After the dermatological procedure, 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
and reduction of erythema after non-ablative lasering on the face.
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.
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