Product Feasibility 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 lens.

Key facts

Study ID

NCT01309100

Run by

Bausch & Lomb Incorporated

People needed

144

Starts

2010-11-01

Expected to finish

2011-01-01

Last updated by the study team

2014-04-29

Who can join

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

You may qualify if…

• Subjects must have clear central corneas and be free of any anterior segment disorders.
• Subjects must be adapted wearers of soft contact lenses, wear a lens in each eye, and each lens must be of the same manufacture and brand.
• Subjects must be myopic and require lens correction

You may not qualify if…

• Subjects with any systemic disease affecting ocular health.
• Subjects using any systemic or topical medications that will, in the Investigator's opinion, affect ocular physiology or lens performance.
• Subjects with an active ocular disease or are using any ocular medication.
• Subjects with any "Present" finding during the slit lamp examination that, in the Investigator's judgment, interferes with contact lens wear.

Where it is running

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

Full record on ClinicalTrials.gov

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