drugset / Trial / NCT01657266

Efficacy and Safety of PRO-155 Versus Nevanac in Post Phacoemulsification

NCT01657266

Phase 2 Completed 160 enrolled Laboratorios Sophia S.A de C.V.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate efficacy and safety of the ophthalmic solution PRO-155 in patients post phacoemulsification.

Timeline

Start
2013-12
Primary completion
2015-03
Completion
2015-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Bromfenac Other / unclassified 0.09 % Other
Comparator Nepafenac Other / unclassified 0.1 % Other