A study to see the efficacy of the lotion (Development code:K8284410) on facial skin condition with Japanese wome
Not Applicable
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000020492
- Lead Sponsor
- Kao Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Subjects with severe systemic diseases and/or skin diseases Subjects who are pregnant and/or who had a childbirth within 2 years Subjects who are receiving hormone therapies Subjects who have laser treatments for facial pigmentation (spot, bruise, etc.), acne etc. Subjects with severe sunburn or subjects who might possibly severe sunburn during the test period Subjects with sensitive skins Subjects seemed to be inappropriate to participate in this study according to the decision by investigators and/or doctors
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of dermatological assessment, measurement of skin color and that of skin shape before and after the repeated treatments of the lotions for 4 and 8 weeks.
- Secondary Outcome Measures
Name Time Method