Evaluation of safety and usefulness of the wearable device for skin bioinstrumentatio
Not Applicable
- Conditions
- 1) Healthy adult 2) The person given informed consent in writing
- Registration Number
- JPRN-UMIN000022800
- Lead Sponsor
- Department of Dermatology, Keio University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
The person with any severe skin symptoms in the study-site and with a serious cardiac and/or muscular disease. The person who have a metal allergy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of an allergic reaction and a primary irritant reaction, based on the criteria of the International Contact Dermatitis Research Group after seven days of an examination.
- Secondary Outcome Measures
Name Time Method Evaluation of the influence to the three-dimensional shape of the skin (roughness, irregularity, etc.)