diabetic retinopathy, diabetic macular edema, central retinal vein occlusion, branch retinal vein occlusion, age-related macular degeneration, myopic choroidal neovascularization, central serous chorioretinopathy, idiopathic choroidal neovascularization
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who are diagnosed as below: diabetic retinopathy, diabetic macular edema, central retinal vein occlusion, branch retinal vein occlusion, age-related macular degeneration, myopic choroidal neovascularization, central serous chorioretinopathy, idiopathic choroidal neovascularization. Patients provided informed written consent before participation and agreed to participate to this study. Patients who can read alphabet.
Exclusion criteria
Exclusion criteria: Patients with congenital color-vision deficiencies Patients who refused to participate this study, or patients who are judged to be unfit as the participants of this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The results of cone contrast test before and after treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation between Cone contrast test and visual acuity Correlation between Cone contrast test and optical coherence tomography findings | — |
Countries
Japan
Contacts
Shiga University of Medical Science Department of Ophthalmology