Healthy adults
Conditions
Interventions
Apply the formulation including an active ingredient to the one side of thigh and the placebo to other side of thigh twice a day for 12 weeks
Sponsors
Kao Corporation
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Healthy females
Exclusion criteria
Exclusion criteria: -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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Thigh circumference and subcutaneous fat layer thickness at 0, 6 and 12 weeks after the topical application. | — |
Countries
Japan
Contacts
Public ContactErina Maeyama
Kao Corporation Biological Science Research
Outcome results
None listed