Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects



Status:Completed
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:November 2009
End Date:April 2010

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This study will evaluate the safety, efficacy, and acceptability of two artificial tears
compared to a currently available artificial tear in subjects with dry eye.


Inclusion Criteria:

- Current use of an artificial tear at least twice daily, for at least three months
prior to Day 1, on average

- Ability/agreement to wear habitual correction (glasses) during study period

Exclusion Criteria:

- Known allergy or sensitivity to the study product(s) or its components

- Anticipate contact lens wear during the study, or subject has worn contact lenses in
the last six months

- Chronic use of systemic medications which may affect a dry eye condition

- Active ocular allergy or infection

- Use of Restasis® or other topical cyclosporine products within 3 months prior to Day
1

- Current use of any topical ophthalmic medications, have used within 2 weeks prior to
Day 1, or are likely to use during study.
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