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Prolensa (Bromfenac) 0.07% QD vs. Ilevro (Nepafenac) 0.3% QD for Treatment of Ocular Inflammation Post Cataract Surgery — QD  

Inflammation Clinical Trial

Official title:
Clinical Outcomes of Prolensa (Bromfenac Ophthalmic Solution) 0.07% QD vs. Ilevro (Nepafenac Ophthalmic Suspension) 0.3% QD for Treatment of Ocular Inflammation Associated With Cataract Surgery

Clinical Trial Summary

To investigate inflammation, visual acuity and macular thickness after treatment with Prolensa vs Ilevro after cataract surgery.

Clinical Trial Description

To investigate the clinical outcomes for inflammation, visual acuity and macular thickness after treatment with Prolensa (bromfenac ophthalmic solution) 0.07% QD in subjects who have undergone cataract extraction with posterior chamber intraocular lens implantation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01847638
Study type Interventional
Source Toyos Clinic
Contact
Status Completed
Phase N/A
Start date April 1, 2013
Completion date August 23, 2018
View Details
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