Feasibility of a New Silicone Hydrogel Lens

Bausch + Lomb

Status

Completed

Conditions

Myopia

Treatments

Device: Investigational contact lens

Device: Air Optix Aqua

Device: Acuvue Oasys Contact Lens

Study type

Interventional

Funder types

Industry

Identifiers

NCT01131130

655

Details and patient eligibility

About

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.

Enrollment

120 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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.

Exclusion criteria

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.