Two Daily Disposable Contact Lenses in Symptomatic Patients



Status:Completed
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:10/5/2018
Start Date:August 13, 2018
End Date:September 25, 2018

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The purpose of this study is to evaluate the performance of ACUVUE OASYS® 1-DAY and DAILIES
TOTAL1® with respect to visual acuity, dryness and discomfort in a symptomatic study
population of monthly or bi-weekly replacement lens wearers.


Inclusion Criteria:

- Able to understand and must sign an IRB-approved informed consent form;

- Soft contact lens wearers in both eyes during the past 3 months;

- Best-corrected visual acuity (BCVA) 20/25 or better in each eye;

- Willing to wear study lenses at least 3 days per week and at least 8 hours per day;

- Willing to stop wearing habitual contact lenses for the duration of study
participation;

- Other protocol-specified inclusion criteria may apply.

Exclusion Criteria:

- Infection, inflammation, abnormality, condition, disease, surgery, or use of
medications, as specified in the protocol;

- Intolerance, hypersensitivity, or allergy to any component of the study products;

- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in
lenses for at least 1 night per week) over the last 3 months prior to enrollment;

- Monocular (only one eye with functional vision);

- Other protocol-specified exclusion criteria may apply.
We found this trial at
4
sites
Bloomington, Illinois 61701
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Bloomington, IL
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Pittsburg, Kansas 66762
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Pittsburg, KS
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Powell, Ohio 43065
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Powell, OH
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Warwick, Rhode Island 02888
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Warwick, RI
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