Male/female adults
Conditions
Interventions
None listed
Sponsors
CPCC Company Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Males and females aged 20 years to less than 60 years from informed consent to the end of the study. 2. Individuals who are able to present to the designated facility on the scheduled visit day for Health Examination 2. 3. Individuals who self-aware of having dry skin. 4. Individuals who are able to give informed consent to participate in this study after receiving a detailed explanation of the protocol and understanding its contents.
Exclusion criteria
Exclusion criteria: 1. Subjects whose systolic blood pressure is less than 90 mmHg 2. Subjects who are participating in other clinical studies, or who finished clinical study within 4 weeks. 3. Subjects who are applicable to following items a) Subjects with disease on heart, liver, kidney or other organs complication. b) Subjects with a previous history of disease on circulatory organs. c) Subjects who are contracting diabetes. d) Subjects with a history of cancer, tuberculosis, or other serious illness 4. Smoker 5.Subjects who drink a lot. 6. Subjects who are judged as unsuitable for the study by the principal investigator for other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Transepidermal Water Loss (TEWL), Stratum Corneum Hydration (SCH), and Subjective Skin Assessment Questionnaire scores | — |
Countries
Japan
Contacts
Public ContactMasanori Numa
CPCC Company Limited Clinical Planning Department
Outcome results
None listed