drugset / Trial / NCT00818844

Role of Nepafenac in Reducing Macular Volume After Epiretinal Membrane Surgery

NCT00818844

Phase 4 Completed 40 enrolled Alcon Research
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to compare the macular volume of patients treated with a 3-month course of topical Nepafenac (0.1% solution) to patients treated with a placebo course following epiretinal membrane surgery.

Timeline

Start
2009-01
Primary completion
2010-06
Completion
2010-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Nepafenac Other / unclassified 0.1 % Topical

Indications