Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Fort Worth, Texas 76134


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.


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.



Primary Contact:

Study Director
Lakeisha Sykes, DMH, MPH
Alcon Research

Backup Contact:


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: March 16, 2018

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.

Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.