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 |
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.
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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