Clinical Research Directory

Inclusion Criteria: * Sex: female and male; * Age : 18 years old and above; * Phototype: I to IV; * Type: Caucasian; * Subjects with active eczema condition the body (showing flakiness, irritation, itch and intense dryness); * Subjects with a SCORAD of 25 - 50; * Local EASI score of 0-15: * 30% - 4-5 * 30%- 6-7 * 30% - 8-9 * Subjects with dry and very dry skin on the study areas (cutaneous hydration rate \< 50 A.U); * Subjects must not take antibiotics and / or apply any antifungal treatments (body/scalp) for 1 month before study start and during the entire study duration; * No change in hygiene, cosmetics, and make-up habits - except for the product(s) under study - during the entire study duration; * Subjects agreeing not to change lifestyle habits during the study duration * Healthy subject; * Subject having given her free informed, written consent; * Subject willing to adhere to the protocol and study procedures; * Subject with Polish citizenship. Exclusion Criteria: * For women with childbearing potential: pregnant or nursing woman or woman planning to get pregnant during the study; * Cutaneous pathology on the study zone (other than eczema); * Use of topical or systemic treatment during the previous weeks liable to interfere with the assessment of the cutaneous acceptability/efficacy of the study product (the subjects are allowed to use their topical corticosteroids during the study if needed; the information about the treatment and the number of applications must be noted in the daily log); * Subject having undergone a surgery under general anesthesia within the previous month; * Excessive exposure to sunlight or UV-rays within the previous month; * Subject enrolled in another clinical trial during the study period (concerns the studied zones).