Expired Study
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Fort Worth, Texas 76134


Purpose:

The purpose of this study is to evaluate cholesterol sorption by Air Optix® Aqua lenses compared to ULTRA lenses after 30 days of wear.


Criteria:

Inclusion Criteria: - Sign informed consent document; - Vision correctable to 20/40 Snellen (feet) or better in each eye at distance with both study contact lenses; - Willing to wear study lenses on a daily basis (minimum 5 days/week, 8 hours/day) and attend all study visits; - Successful wear of single-vision spherical, 2-week/ monthly replacement silicone hydrogel contact lenses in both eyes daily wear during the past 2 months for a minimum of 5 days/week, 8 hours/day. (Note: Monovision is included); - Other protocol-specified inclusion criteria may apply. Exclusion Criteria: - Any anterior segment infection, inflammation, disease or abnormality that contraindicates contact lens wear (within 7 days of enrollment, or current); - History of herpetic keratitis, corneal surgery or irregular cornea; - Any use of systemic or ocular medications within the past 30 days for which contact lens wear could be contraindicated as determined by the investigator; - Monocular (only 1 eye with functional vision) or fit with only one lens; - Current or past Air Optix® Aqua or Ultra lens wearers; - Other protocol-specified exclusion criteria may apply.


NCT ID:

NCT02495948


Primary Contact:

Study Director
Clinical Trial Manager, Vision Care, GCRA
Alcon Research


Backup Contact:

N/A


Location Contact:

Fort Worth, Texas 76134
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 19, 2017

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