A Study to Evaluate the Performance of Two Designs of Soft Toric Lenses

Completed · Not applicable

Conditions studied: Myopia

In brief

The objective of the study is to evaluate the product performance of the Bausch + Lomb toric investigational contact lenses compared to the currently marketed PureVision toric contact lenses.

Key facts

Study ID

NCT01309867

Run by

Bausch & Lomb Incorporated

People needed

302

Starts

2010-12-01

Expected to finish

2011-04-01

Last updated by the study team

2020-10-08

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 lens wearers, 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
• Subjects must be habitual wearers of toric soft contact lenses.

You may not qualify if…

• Subjects with any systemic disease currently affecting ocular health or which in the Investigator's opinion may have an effect on ocular health during the course of the study.
• 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 who are using any ocular medication.
• Subjects with any grade 2 or greater finding during the slit lamp examination. Subjects with corneal infiltrates, of ANY GRADE, are not eligible.
• Subjects with any "Present" finding during the slit lamp examination that, in the Investigator's judgment, interferes with contact lens wear.
• Subjects who are 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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