A study on the dermatological efficacy of oral administration of beauty capsule
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000025667
- Lead Sponsor
- SOUKEN Co., Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 30
Not provided
-Subjects who go to hospital regularly or went to hospital within the past 1 month for disease: skin, gastrointestinal system, liver, kidney, heart, blood pressure, and physical deconditioning. (Manual therapeutics, chiropractic and massage are not included.) -Subjects who are routinely taking oral medicine or applying external use medicine (ex. hypnotic, analgesic, anti-histamine, rhinitis drug, hormone preparation, cathartic, intestinal regulator, and others). -Subjects who have received medical cosmetic treatment before. -Subjects who have food or drug allergies. -Subjects who are pregnant, could be pregnant in near future, or are breast feeding. -Subjects who are participating in another clinical study. -Subjects who are 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 Evaluation of skin properties, e.g. skin color, transepidermal water loss, and skin hydration and blood parameters before and after capsule intake.
- Secondary Outcome Measures
Name Time Method