Healthy volunteers who were enrolled to this study after they signed an informed consent form and provided written and oral information to the study physicians.
Conditions
Interventions
with or without histamine
Sponsors
Dept. of dermatology, Osaka university
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Subjects with signed an informed consent form and provided written and oral information to the study physicians.
Exclusion criteria
Exclusion criteria: - The part-time-service personnel, a fixed-term employment person - Whose consent was not obtained -Subjects with glaucoma, cholinergic urticaria, asthma, prostatic hypertrophy, a pregnant woman, the woman under breast-feeding -Subjects with dermatoses in a test lesion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) axon-reflex mediated sweating volume 2) latency time | — |
Countries
Japan
Contacts
Public Contact0668795111
Osaka univeristy Dermatology
Outcome results
None listed