A Study to Evaluate a New Silicone Hydrogel Contact Lens

Completed · Not applicable

Conditions studied: Myopia

In brief

The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses.

Key facts

Study ID

NCT01309893

Run by

Bausch & Lomb Incorporated

People needed

66

Starts

2010-12-01

Expected to finish

2011-02-01

Last updated by the study team

2014-11-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Have physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings.
• Be myopic and require lens correction from -0.50 D to -5.50 D in each eye.

You may not qualify if…

• Any systemic disease affecting ocular health.
• Using any systemic or topical medications that will affect ocular physiology or lens performance.
• An active ocular disease, any corneal infiltrative response or are using any ocular medications.
• Any "Present" finding during the slit lamp examination that, in the Investigator's judgment, interferes with contact lens wear.
• Allergic to any component in the study care products.

Where it is running

• Bausch & Lomb — Rochester, New York, United States

Full record on ClinicalTrials.gov

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