chronic central serous chorioretinopathy
Conditions
Interventions
ranibizumab pegaputanib aflibercept
Sponsors
Kansai medical university medical center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Willingness to provide written informed consent 2) Chronic CSC on fluorescein angiography (FA), indocyanine green angiography (IA), optical coherence tomography (OCT)
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) Ratio of patients with improved/maintained best-corrected visual acuity (BCVA) at month 1,3,6,12 2) Ratio of patients with improved central retinal thickness (CRT) at month 1,3,6,12 | — |
Secondary
| Measure | Time frame |
|---|---|
| Change of BCVA, CRT etc. | — |
Countries
Japan
Contacts
Public ContactTsuyoshi Otsuji
Kansai medical university medical center Department of Ophthalmology
Outcome results
None listed