Clinical Evaluation of Two Daily Disposable Silicone Hydrogel Contact Lenses

Completed · Not applicable

Conditions studied: Myopia

In brief

The purpose of this crossover study was to evaluate the end-of-day comfort of two commercially available, daily disposable, silicone hydrogel contact lenses.

Key facts

Study ID

NCT01561560

Run by

Alcon Research

People needed

123

Starts

2012-05-01

Expected to finish

2012-08-01

Last updated by the study team

2014-01-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Sign written Informed Consent Document.
• Currently wearing soft contact lenses in both eyes and identified as symptomatic based on questionnaire responses.
• Currently wearing either daily disposable contact lenses or weekly/monthly replacement contact lenses.
• Able to achieve visual acuity of at least 6/7.5 in each eye with study lenses in the available parameters.
• Willing to wear study lenses for at least eight hours per day and at least five days per week.
• Other protocol-defined inclusion criteria may apply.

You may not qualify if…

• Has not worn contact lenses before.
• Currently wearing DAILIES TOTAL1 or 1-DAY ACUVUE TRUEYE contact lenses.
• Any systemic or ocular disease or disorder that would negatively affect the conduct or outcome of the study.
• Ocular surgery/trauma within the last six months.
• Topical ocular or systemic use of antibiotics within seven days of enrollment.
• Pregnant or nursing women.
• Other protocol-defined exclusion criteria may apply.

Where it is running

• Contact Alcon Call Center for Trial Locations — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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