Comparative study of ultra-high resolution OCT and conventional OCT
Not Applicable
- Conditions
- ormal, retinal disease and glaucoma
- Registration Number
- JPRN-UMIN000031499
- Lead Sponsor
- Mie University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 0
Inclusion Criteria
Not provided
Exclusion Criteria
1. Subjects unable to follow fixation. 2. Subjects with cataract unable to measure. 3. Subjects who have medical history for a side effect by using a mydriatic agent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method