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Residence Time Evaluation of Marketed OTC Ophthalmic Products

NCT00804791 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2012-02-02

No results posted yet for this study

Summary

The objective of this study is to measure ocular surface residence time (in minutes) of two marketed OTC ophthalmic products in dry eye patients.

Conditions

  • Dry Eye

Interventions

OTHER

Systane Ultra Lubricant Eye Drops

artificial tears solution for lubricating the cornea

OTHER

Unisol 4 Saline Solution

saline solution for irrigating the cornea

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2009-02-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00804791 on ClinicalTrials.gov