Efficacy test of the topical agent CIB01
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000029581
- Lead Sponsor
- Kao Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 25
Not provided
-Subjects who went to a hospital or been received medication for treatment of diseases within the last 1 month. -Subjects with a history or have been suffered from cardiovascular disease (Such as irregular pulse, angina pectoris, cardiac insufficiency). -Subjects who are pregnant, planning a pregnancy and lactating. -Subjects who are more sensitive to soaps, alcohol, velcro, adhesive tape, water-based gel, or permanent marker ink. -Subjects who underwent liposuction. -Subjects who had weight change of more than 5 kg within the last 3 months. -Subjects with atopic dermatitis, contact dermatitis, cutaneous hypersensitivity, any type of skin condition (such as eczema, skin irritation, or skin infection) -Subjects who participated in another clinical study applying agent or performing tape stripping to test site during this study or within 1 month before this study. -Subjects who participated in another clinical study eating foods during this study or within 1 month before this study. -Subjects who recieved special body care treatment for legs such as application of slimming cosmetics, massage by cosmetic instruments and esthetic treatment during this study or within 1 month before this study. -Subjects who have been suffered from a critical disease. -Subjects 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
- Secondary Outcome Measures
Name Time Method