Expired Study
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Fort Worth, Texas 76134


Purpose:

The purpose of this study is to measure the coefficient of friction of three silicone hydrogel daily disposable contact lenses (1-DAY ACUVUE® TruEye®, MyDay™ and clariti® 1day) after 16 hours of wear.


Study summary:

In this 3-treatment, 3-period, 6-sequence crossover study, each participant will wear all 3 products in randomized order, 1 product at a time, with a washout period of up to 7 days between treatment periods. Lenses will be collected for ex-vivo lubricity analysis. The ex-vivo lubricity analysis will be conducted under a separate non-clinical protocol.


Criteria:

Inclusion Criteria: - Must sign an informed consent form. - Soft contact lens wearer (both eyes). - Willing to wear study lenses at least 16 waking hours and attend all study visits. - Other protocol-specified inclusion criteria may apply. Exclusion Criteria: - Ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear. - Use of systemic or ocular medications for which contact lens wear could be contraindicated. - Use of artificial tears and rewetting drops during the study. - Monocular (only 1 eye with functional vision) or fit with only 1 lens. - History of herpetic keratitis, ocular surgery, or irregular cornea. - Pregnant. - Other protocol-specified exclusion criteria may apply.


NCT ID:

NCT02402127


Primary Contact:

Study Director
Lakeisha Sykes, DMH, MPH
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 23, 2017

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