Eylea and Lucentis for Macular Edema in Branch Retinal Vein Occlusion
Launched by ST. ERIK EYE HOSPITAL · Oct 15, 2018
Trial Information
Current as of April 24, 2025
Completed
Keywords
ClinConnect Summary
One hundred and ten patients with macular edema (ME) secondary to BRVO are randomized (1:1) to treatment with intravitreal injections of aflibercept or ranibizumab. An initial loading dose of at least three monthly injections is given in the study eye until the ME is resolved. Then patients are observed at regular intervals, initially every four weeks until study completion. Total follow-up time is nine months from baseline to completion. If ME recurs, patients are treated according to a treat-and-extend algorithm.
At every visit, visual acuity (VA) is measured with an ETDRS chart at 4 m. ...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • BRVO naïve patients, disease duration 1-6 months, BCVA 23-73 ETDRS letters (20/40-20/320), macula edema with intraretinal cysts and CRT \> 300 micrometers (Cirrus)
- Exclusion Criteria:
- • BRVO with neovascular component, intraocular surgery during the previous 3 months, earlier vitreoretinal surgery, vascular retinopathy of other cause, intraocular infection/inflammation, myocardial infarction och cerebrovascular stroke during the last 3 months.
Trial Officials
Anders Kvanta, MD PhD
Principal Investigator
St. Erik Eye Hospital
About St. Erik Eye Hospital
St. Erik Eye Hospital is a leading specialized ophthalmic center dedicated to advancing eye care through innovative research and clinical trials. As a prominent sponsor of ophthalmology studies, the hospital focuses on enhancing patient outcomes by exploring new treatment modalities and technologies. With a commitment to excellence in patient care and a collaborative approach involving multidisciplinary teams, St. Erik Eye Hospital strives to contribute significantly to the field of vision science and improve the quality of life for individuals with various eye conditions.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Stockholm, , Sweden
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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