Examination of stimulation brightness of multi-focal ERG recording without mydriasis (under non-mydriasis)
Not Applicable
- Conditions
- ormal eye
- Registration Number
- JPRN-UMIN000046695
- Lead Sponsor
- ational Hospital Organization Osaka National Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
Exclude those with a predisposition to increase intraocular pressure, such as glaucoma, narrow angle, and shallow anterior chamber. Exclude those with a history of hypersensitivity to the components of the drugs used (Tropicamide, Phenylephrine Hydrochloride, Oxybuprocaine Hydrochloride ophthalmic solution) and benzoic acid ester-based local anesthetics.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method