IRB Number
|
#19381
|
| Description |
This study is comparing two
treatments for people with central retinal vein occlusion or branch retinal
vein occlusion. |
| What is expected of me? |
Participation in this research
study will receive either standard care or intravitreal injections. |
| Inclusion Criteria |
Center involved macular edema from CRVO or BRVO
documented for 2-18 months, visual acuity of 20/40 to 20/320 |
| Exclusion Criteria |
Allergic to corticosteroid, systemic use of
corticosteroids during the last 4 months, prior grid laser for macular
edema, prior intravitreal; corticosteroid injection |
| Length of Study |
36 months |
| Study Location |
Penn State Milton S. Hershey
Medical Center |
| Investigator Information |
Dr. Kimberly Neely
Dept. of Ophthalmology |
| To obtain more information about this study please contact: |
Susan Chobanoff
717-531-3790 |
