Clinical Trials Directory

Trials / Completed

CompletedNCT02645747

Retrospective Data Analysis of Patients Treated for Macular Edema Due to Central Retinal Vein Occlusion

RETRO CRVO: Retrospective Data Analysis of Patients Treated for Macular Edema Due to Central Retinal Vein Occlusion

Status
Completed
Phase
Study type
Observational
Enrollment
126 (actual)
Sponsor
Bayer · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this retrospective chart review is to evaluate drug utilization, usage patterns and indication of effectiveness Eylea in the routine clinical (real-life) management of patients who suffer from ME (Macular Edema), secondary to CRVO (Central Retinal Vein Occlusion), and who started treatment with Eylea for this indication.

Conditions

Interventions

TypeNameDescription
DRUGAflibercept (Eylea, BAY86-5321)Eylea (intravitreal aflibercept) is an anti-Vascular Endothelial Growth Factor (VEGF) drug indicated for neovascular age-related macular degeneration (AMD), visual impairment due to diabetic macular edema (DME) and visual impairment due to macular edema (ME) secondary to central or branched retinal vein occlusion (RVO). RVO, both branch and central, is the second most common type of retinal vascular disorders after diabetic retinal disease. Central retinal vein occlusion (CRVO) is characterized by an obstruction of the central retinal vein combined with variable amounts of retinal arterial insufficiency.

Timeline

Start date
2016-01-21
Primary completion
2017-12-23
Completion
2017-12-23
First posted
2016-01-05
Last updated
2018-09-06

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02645747. Inclusion in this directory is not an endorsement.