Overview

Visual Outcomes and the Predictive Factors in Chinese Patients With Diabetic Macular Edema Treated With Ranibizumab

Status:
Unknown status
Trial end date:
2020-01-01
Target enrollment:
0
Participant gender:
All
Summary
The aim of this study is to evaluate the one-year visual outcome and prognostic factors after intraocular injections of ranibizumab under pro re nata treatment regimen for the patients with diabetic macular edema (DME).
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Sun Yat-sen University
Treatments:
Ranibizumab
Criteria
Inclusion Criteria:

- 1) patients (aged>18 years) with DME who had a best-corrected visual acuity (BCVA)
between 20/32 and 20/200, and CRT≥300μm; 2) clinically significant DME confirmed by
both fundus fluorescein angiography (FFA) and optical coherence tomography (OCT)
(Spectralis HRA+OCT; Heidelberg Engineering, Germany); 3) decreased vision caused by
foveal thickening from DME, which could not be explained by any other cause.

Exclusion Criteria:

- 1) previous anti-VEGF or laser treatment; 2) proliferative diabetic retinopathy who
required immediate panretinal photocoagulation; 3) active proliferative diabetic
retinopathy; 4) other causes for macular edema, for example, branch retinal vein
occlusion; 5) other causes of visual loss in the study; 6) unstable systemic
conditions, for example, uncontrolled blood pressure, stroke, renal or kidney failure.