Atopic dermatitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ?Japanese females aged from 25 to less than 50 years old at the time informed consent was provided ?Subjects with very mild or mild dry skin and desquamation, and with low skin moisture as measured by a screening test ?Voluntary study participants who provided written informed consent
Exclusion criteria
Exclusion criteria: ?Subjects with moderate or greater atopic dermatitis, sebum deficiency, or xeroderma on the face ?Subjects with mild or greater redness/erythema on the face ?Subjects using a topical steroid or a tacrolimus ointment on the face ?Subjects using a medical-use topical moisturizer on the face ?Subjects receiving systemic administration of steroids or immunosuppressive agents ?Subjects with allergies to cosmetics or foods ?Pregnant women, those who may be pregnant, lactating women, or women who hope to become pregnant during the study period ?Subjects who has participated in other human studies within the past four weeks, or subjects who plan to participate in other human studies during the planned period of the study ?Subjects who were considered inappropriate for the study by an investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of dermatological assessment and questionnaire before and after the repeated use of clear facial lotion and milky facial lotion for 1, 4, 6, and 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Measurement of transepidermal water loss (TEWL) and skin moisture | — |
Countries
Japan
Contacts
DRC Co., Ltd. Product Testing Department