Clinical Trials Directory

Trials / Completed

CompletedNCT01375582

Objective Evaluation of Ocular Surface Lubricants in Two Environments

Objective Evaluation of Ocular Surface Lubricants

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
University of Rochester · Academic / Other
Sex
All
Age
30 Years – 75 Years
Healthy volunteers
Accepted

Summary

This study will evaluate ocular surface lubricants in subjects with dry eye syndrome.

Detailed description

This study will objectively evaluate ocular surface lubricants in subjects with dry eye syndrome. Lubricants contain compounds that are purported to improve dry eye symptoms, although objective data is not available. The investigators seek to objectively evaluate the effectiveness of two lubricants and compare the results to a saline eye drop (control). The investigators will assess the lipid layer before and after the administration of three products in the same eye of 25 dry eye subjects using the ellipsometry, imaging in a "normal" environment. Subsequently the investigators will change the environment to one that causes the subjects' ocular surface to experience "evaporative stress" (warmer, less humid and greater air flow) and perform the before and after drop administration measurements with the same three products in the same eye as the first environment.

Conditions

Interventions

TypeNameDescription
DRUGB & L Soothe Lubricant Eye DropsEye Drop
DRUGLiposic EDOEye Drop
DRUGOcuFresh Eye WashSaline drop

Timeline

Start date
2011-06-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2011-06-17
Last updated
2022-11-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01375582. Inclusion in this directory is not an endorsement.