The purpose of this study is to test the efficacy and safety of AzA 15% Gel in the treatment of mild to moderate perioral dermatitis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
48
gel, applied once daily, for 6 weeks
gel, apply once daily for six weeks
Unnamed facility
Berlin, Germany
Unnamed facility
Dülmen, Germany
Unnamed facility
Essen, Germany
Unnamed facility
Recklinghausen, Germany
The sum score derived from the most important signs and symptoms of perioral dermatitis
Time frame: Measurements and observations during the course of the study
Intensity of single signs and symptoms
Time frame: Measured at scheduled visits during the course of the study
Safety outcomes measures will be all adverse events reported by the patients or observed by the investigator
Time frame: Safety parameters recorded at scheduled visits during the course of the study
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