Lubricity Post-Wear - Competitive Lenses Pilot



Status:Completed
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:May 2015
End Date:July 2015

Use our guide to learn which trials are right for you!

Trial Summary
Trial Overview
Inclusion Criteria

Lubricity Post-Wear - Pilot Evaluation of Daily Disposable Silicone Hydrogel Contact Lenses After Wear

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.

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.
We found this trial at
1
site
Contact Alcon Call Center for Trial Locations
Fort Worth, Texas 76134
?
mi
from
Fort Worth, TX
Click here to add this to my saved trials