Lubricity Post-Wear - Competitive Lenses Pilot

Status Completed

Clinical Trial Summary

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.

Clinical Trial Description

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. ;

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor)

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02402127
Study type	Interventional
Source	Alcon Research
Contact
Status	Completed
Phase	N/A
Start date	May 2015
Completion date	July 2015

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