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Clinical Trial Details — Status: Recruiting

Administrative data

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

Study information

Verified date August 2015
Source Fukushima Medical University
Contact Akira Ojima, M.D., Ph.D
Phone +81-24-548-2111
Email ao@fmu.ac.jp
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Ranibizumab

Ranibizumab and laser


Locations

Country Name City State
Japan Department of Ophthalmology, Fukushima Medical University Fukushima

Sponsors (1)

Lead Sponsor Collaborator
Fukushima Medical University

Country where clinical trial is conducted

Japan, 

Outcome

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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