Feasibility of a New Silicone Hydrogel Lens

Completed · Not applicable

Conditions studied: Myopia

In brief

The objective of this study is to determine the product feasibility of the investigational contact lens (Test) when compared to the currently marketed Acuvue Oasys contact lens (Control) and the Air Optix Aqua contact lens (Control) when worn by adapted wearers of soft contact lenses.

Key facts

Study ID

NCT01131130

Run by

Bausch & Lomb Incorporated

People needed

120

Starts

2010-05-01

Expected to finish

2010-06-01

Last updated by the study team

2014-04-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants must have clear central corneas and be free of any anterior segment disorders.
• Participants 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.
• Participants must be myopic and require lens correction from -0.75 D to - 4.75D in each eye.

You may not qualify if…

• Participants who have worn gas permeable (GP) contact lenses within the last 30 days or who have worn polymethylmethacrylate (PMMA) lenses within the last three months.
• Participants with any systemic disease affecting ocular health.
• Participants using any systemic or topical medications that will, in the Investigator's opinion, affect ocular physiology or lens performance.
• Participants with an active ocular disease or are using any ocular medication.
• Participants who have had any corneal surgery (eg, refractive surgery).
• Participants 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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