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Safety and Efficacy Study of Dexamethasone in the Treatment of Patients With Macular Edema Following Retinal Vein Occlusion (RVO)

Macular Edema Clinical Trial

Clinical Trial Summary

This study will assess the safety and efficacy of 700 μg dexamethasone Posterior Segment Drug Delivery System (DEX PS DDS) Applicator System in patients with macular edema in a 6 month double-blind period versus sham followed by a 2 month open label period.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01660802
Study type Interventional
Source Allergan
Contact
Status Completed
Phase Phase 3
Start date September 4, 2012
Completion date May 20, 2014
View Details
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