Clinical Trials Directory

Trials / Completed

CompletedNCT00818844

Role of Nepafenac in Reducing Macular Volume After Epiretinal Membrane Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGNepafenac 0.1%NSAID
OTHERBSSBSS

Timeline

Start date
2009-01-01
Primary completion
2010-06-01
Completion
2010-06-01
First posted
2009-01-08
Last updated
2015-08-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00818844. Inclusion in this directory is not an endorsement.

Role of Nepafenac in Reducing Macular Volume After Epiretinal Membrane Surgery (NCT00818844) · Clinical Trials Directory