The effect verification examination by continuous use of bath additives
Not Applicable
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000026027
- Lead Sponsor
- INFORWARD inc. EBISU Skin research center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Subjects who has a cutaneous symptom which affects the final examination in the body (2) Subjects who are using the drugs which may influence an examination (3) Subjects (except for dental care) under a therapy or going to hospital regularly due to sick. (4) Subjects who has pollinosis (5) Subjects past menopause (6) Subjects under pregnancy or who may have been conceived, and breast-feeding (7) Subjects who has participated in other clinical trials (8) Subjects judged that a test implementation person in charge is unsuitable
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of fatigue, sleep, body composition, an autonomic nerve function, a vascular function, and blood composition before use of bath additives and after continuous use for 2 and 4 weeks
- Secondary Outcome Measures
Name Time Method