A study to validate the usefulness of a general-purpose smartphone opthalmoscopy in healthy volunteers
Phase 1
Recruiting
- Conditions
- healthy volunteers
- Registration Number
- JPRN-jRCTs032220697
- Lead Sponsor
- Matsui Hikoro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
1. Men and women over 18 and under 70 years of age
2. Those who have received a full explanation of the study and have given written consent of their own free will based on a full understanding of the study
Exclusion Criteria
1. Those with subjective eye-related symptoms (pain or discomfort even in one eye)
2. Pregnant or lactating women
3. Those with glaucoma, diabetes mellitus or hyperthyroidism
4. Those who have been pointed out to have narrow corner angles
5. Those who are being treated with MAO inhibitors or within 3 weeks after treatment
6. Those on treatment with tricyclic and tetracyclic antidepressants
7. Those who are judged inappropriate for participation in this study by the principal investigator or co-investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method