Healthy adult Female
Conditions
Interventions
Use test articles (facial equipment) on one side of the face for 8 weeks
The other side of the face, no using test article
Sponsors
Japan Clinical Trial Association
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Subjects that correspond to one or more of dry skin, enlarged pores, dull skin, and lack of firmness of the skin
Exclusion criteria
Exclusion criteria: 1.Those who are pregnant or may be pregnant, and those who are breastfeeding 2.Persons who work night shifts or day and night shifts 3.Subjects whose wake-up time and bedtime fluctuate by 4 hours or more depending on the day of the week 4.Individuals who need help from others and are unable to walk independently. 5.Subjects participating in other clinical trials 6.Factors that may affect the test results (disease such as atopic dermatitis and urticaria, inflammation, eczema, trauma, acne, tumor warts with a diameter of 5 cm or more on the cheek, etc.) , or traces of it) 7.Subjects who are judged as unsuitable for the study by the investigator for the other reason
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of devices that measure (Before use / Immediately after use / 4 weeks later / 8 weeks later) | — |
Secondary
| Measure | Time frame |
|---|---|
| subjective assessment | — |
Countries
Japan
Contacts
Public ContactTakeshi Kaneko
Japan Clinical Trial Association N.A.
Outcome results
None listed