A Study to Evaluate the Product Performance of the PureVision®2 High Definition (HD) Contact Lens

Completed · Not applicable

Conditions studied: Myopia

In brief

The objective of this study is to evaluate the product performance of PureVision2 HD contact lenses.

Key facts

Study ID

NCT01416142

Run by

Bausch & Lomb Incorporated

People needed

63

Starts

2011-07-01

Expected to finish

2011-09-01

Last updated by the study team

2013-12-25

Who can join

Age: 15 and older, up to 30. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Have physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings
• Subjects must be myopic or hyperopic and require lens correction in each eye
• Subjects must own a pair of spectacles and the spectacle prescription must have been updated or confirmed as correct within the last 2 years.

You may not qualify if…

• Any "Present" finding during the slit lamp examination that, in the Investigator's judgment, interferes with contact lens wear.
• Any systemic disease affecting ocular health.
• Using any systemic or topical medications that will affect ocular physiology or lens performance.
• Allergic to any component in the Biotrue multi-purpose solution

Where it is running

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

Full record on ClinicalTrials.gov

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