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Search / Trial NCT03709745

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.

Locations

Stockholm, , Sweden

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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