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
| Type | Name | Description |
|---|---|---|
| OTHER | Ophthalmic dye | Topically instilled for the purpose of assessing lid margin staining |
| DEVICE | Contact lenses | Silicone 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.