Branch Retinal Vein Occlusion Clinical Trial
Official title:
Retinal Sensitivity in Branch Retinal Vein Occlusion After Anti-VEGF Therapy
NCT number | NCT02527733 |
Other study ID # | 2129 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 4 |
First received | June 29, 2015 |
Last updated | August 17, 2015 |
Start date | June 2015 |
The efficacy of anti-vascular endothelial growth factor (VEGF) therapy for branch retinal vein occlusion (BRVO) is shown, but its effect on retinal sensitivity is not fully investigated. The purpose of this study is to compare the changes in retinal sensitivity after ranibizumab therapy or combination therapy of ranibizumab and laser photocoagulation in eyes with BRVO.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | |
Est. primary completion date | September 2017 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Treatment naive patients of branch retinal vein occlusion with visual acuity of less than 1.0 and macular edema of more than 250 micrometers in foveal thickness. Exclusion Criteria: - Patients with history of treatment for branch retinal vein occlusion, possibility of pregnancy, allergy for ranibizumab, intraocular infection, or severe inflammation will be excluded. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Japan | Department of Ophthalmology, Fukushima Medical University | Fukushima |
Lead Sponsor | Collaborator |
---|---|
Fukushima Medical University |
Japan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Retinal sensitivity measured by microperimetry (MP-3, NIDEK, Japan) | At 12 months | No |
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