Formula Identification (FID) 114657 in Contact Lens Wearers

Launched by ALCON RESEARCH · Nov 17, 2014

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Must sign the informed consent form.
• • Stable, tear lipid layer thickness ≤ 75 nm without contact lenses.
• • Successfully wearing bi-weekly or monthly replacement soft contact lenses in both eyes for a minimum of 5 days/week during the past 2 months prior to Visit 1.
• • Vision correctable to 20/25 Snellen (feet) or better at distance with habitual contact lenses at Visit 1.
• • Willing to wear lenses 5 days a week, 8 hours a day for at least 2 days during the study.
• • Demonstrate symptoms of contact lens discomfort.
• • Other protocol-defined inclusion criteria may apply.
• Exclusion Criteria:
• • Routinely sleeping in lenses.
• • Any active eye inflammation or condition that contraindicates contact lens wear.
• • Any systemic diseases that could prevent successful contact lens wear.
• • Use of systemic or ocular medications that contraindicate lens wear.
• • Fit with only 1 contact lens.
• • Unwilling to discontinue the use of cosmetics (such as eyeliner, mascara, or eye shadow) or facial creams on or around the eyelids on Day 1 and Day 14 of the study.
• • Women of childbearing potential who are currently pregnant, test positive for pregnancy at Screening visit, breast feeding, or unwilling to use adequate birth control throughout the study.
• • Other protocol-defined exclusion criteria may apply.