Study of the effect of occlusion on the skin.
Not Applicable
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000035367
- Lead Sponsor
- Kao Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 12
Inclusion Criteria
Not provided
Exclusion Criteria
1) Persons with skin disease history (e.g. atopic dermatitis, contact dermatitis), or with cutaneous hypersensitivity. 2) Persons whose test sites are not left in both volar forearms for some reason. 3) Persons who participated in the clinical test within one month. 4) Persons deemed inappropriate to participate in this study by the principle investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Daily changes in trans-epidermal water loss value from after the SC damage to recovery.
- Secondary Outcome Measures
Name Time Method Changes in skin surface conditions (structure, color), Changes in the structure of skin blood capillaries, and the skin blood flow.