Study on safety of Transcorneal electrical stimulation for healthy subjects
Not Applicable
- Conditions
- volunteer(healthy)
- Registration Number
- JPRN-UMIN000028359
- Lead Sponsor
- Ophthalmology, University of Miyazaki hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
Not provided
Exclusion Criteria
1) Target who judged that the person responsible for implementation was inappropriate as a subject. 2) If you discover an optic nerve disease before starting the study, you will stop participating in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in visual function before and after TES use
- Secondary Outcome Measures
Name Time Method Changes before and after TES use of pupil, light reaction, visual field, fundus photograph, OCT, papillary retinal blood flow, VEP, PhNR