Clinical Trials Directory

Trials / Completed

CompletedNCT01611922

Optimization of Assessment and Grading for Lid Wiper Epitheliopathy

Status
Completed
Phase
Study type
Observational
Enrollment
57 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
17 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to assess eyelid margin staining, termed "lid wiper epitheliopathy" (LWE), in three populations. The hypothesis is LWE will be more prevalent in symptomatic contact lens wearers than non-symptomatic contact lens wearers and least prevalent in asymptomatic non-contact lens wearers.

Conditions

Interventions

TypeNameDescription
OTHEROphthalmic dyeTopically instilled for the purpose of assessing lid margin staining
DEVICEContact lensesSilicone hydrogel contact lenses per subject's habitual brand and power, worn for a minimum of 8 hours on the day of assessment, after which lenses will be removed and dye will be instilled.

Timeline

Start date
2012-04-01
Primary completion
2012-05-01
Completion
2012-05-01
First posted
2012-06-05
Last updated
2012-06-05

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01611922. Inclusion in this directory is not an endorsement.