This study will assess the safety and efficacy of FA Intravitreal Inserts in subjects with macular edema secondary to RVO.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
20
0.2 µg/day
0.5 µg/day
University of Kentucky Department of Ophthalmology
Lexington, Kentucky, United States
Ophthalmic Consultants of Boston
Boston, Massachusetts, United States
Cole Eye Institute
Cleveland, Ohio, United States
Visual Acuity
To compare the 3 month best corrected visual acuity to baseline in subjects diagnosed with macular edema secondary to retinal vein occlusion. BCVA will be measured according to the standard procedure developed for ETDRS at 4 meters or 3 meters if the electronic (E)-ETDRS system is employed.
Time frame: 3 months
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