1) Healthy adult 2) The person given informed consent in writing
Conditions
Interventions
to confirm the adverse effect, when a newly developed wearable device are loaded on the skin
Sponsors
Department of Dermatology, Keio University School of Medicine
Department of Electrical and Electronic Engineering, School of Engineering, the University of Tokyo
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy adult volunteers who declare the consent in writing for participating in this study.
Exclusion criteria
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Evaluation of the influence to the three-dimensional shape of the skin (roughness, irregularity, etc.) | — |
Countries
Japan
Contacts
Public ContactTamotsu Ebihara
Keio University School of Medicine Department of Dermatology
Outcome results
None listed