Safety and Efficacy of a Contact Lens for Daily Disposable Use

Completed · Not applicable

Conditions studied: Myopia

In brief

This study is to evaluate the safety and efficacy of a new hydrogel daily disposable contact lens compared to the Bausch + Lomb SofLens® daily disposable contact lens when worn by current soft contact lens wearers on a daily disposable wear basis.

Key facts

Study ID

NCT01365039

Run by

Bausch & Lomb Incorporated

People needed

173

Starts

2011-06-01

Expected to finish

2011-10-01

Last updated by the study team

2014-01-08

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must be myopic and require lens correction from -0.50 D to -6.00 D in each eye.
• Subjects must be correctable through spherocylindrical refraction to 40 logMAR letters or better (distance, high contrast) in each eye.
• Subjects must be free of any anterior segment disorders.
• Subjects must be adapted soft contact lens wearers and agree to wear their study lenses on a daily disposable wear basis for approximately 3 months.

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 any "Present" finding during the slit lamp examination that, in the Investigator's judgment, interferes with contact lens wear.
• Subjects who have had any corneal surgery (eg, refractive surgery).
• Subjects who are allergic to any component in the study care products.

Where it is running

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

Full record on ClinicalTrials.gov

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