Evaluation of 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 developed by Bausch + Lomb.

Key facts

Study ID

NCT01309880

Run by

Bausch & Lomb Incorporated

People needed

66

Starts

2010-12-01

Expected to finish

2011-01-01

Last updated by the study team

2015-02-23

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 adapted wearers of soft contact lenses, wear a lens in each eye, and each lens must be of the same manufacture and brand.

You may not qualify if…

• Have worn gas permeable (GP) contact lenses within last 30 days or polymethylmethacrylate (PMMA) lenses within last 3 months.
• 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, Incorporated — Rochester, New York, United States

Full record on ClinicalTrials.gov

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