A preliminary study to determine the safety and efficacy of intravitreal aflibercept injection in patients with persistent central serous chorioretinopathy.
Intravitreal Aflibercept Injection for Persistent Central Serous Chorioretinopathy: A Prospective Pilot Study
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
12
GROUP A - Aflibercept 2 mg injected at Baseline, Month 1, Month 2, and Month 4 (four injections total). GROUP B - Aflibercept 2 mg injected at Baseline, Month 1, Month 2, Month 3, Month 4, and Month 5 (six injections total).
Mid Atlantic Retina- Huntingdon Valley
Huntingdon Valley, Pennsylvania, United States
Mid Atlantic Retna- Wills Eye Institute
Philadelphia, Pennsylvania, United States
Safety of Intravitreal Aflibercept Injection
Safety will be measured by the amount, significance and details of adverse events/reactions to the study drug.
Time frame: 6 months
Change in Vision Based on Letter Score
• Mean change from baseline in best-corrected ETDRS (Early Treatment of Diabetic Retinopathy Study) letter score
Time frame: 6 months
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