Acute Clinical Evaluation of Multi-purpose Solutions (MPS) in Soft Contact Lens Wearers

Acute Clinical Evaluation of MPS in Soft Contact Lens Wearers

The purpose of this study was to clinically evaluate lens care solutions used with soft contact lenses.

This study was conducted as a series of ten smaller studies in three countries using commercially available contact lens solutions per each country, ie, United Kingdom, France, and the Philippines. In each study, participants were assessed after use of up to 5 products (with one always being a control saline/blister pack solution) in randomized order in conjunction with one of the silicone hydrogel contact lenses. A total of 278 participants were enrolled in the 10 studies.

Inclusion Criteria:

• Have read, understood, signed, and dated the written Informed Consent.
• Be an adapted and successful soft contact lens wearer on a daily wear basis for at least two weeks.
• Vision correctable to at least 20/30 Snellen.
• Other protocol-defined inclusion criteria may apply.

Exclusion Criteria:

• Topical ocular medication use.
• History of hypersensitivity to any component of the study contact lens care systems.
• Any slit-lamp finding of abnormal nature at the baseline visit assessment of each study period.
• Pregnant, lactating, or planning a pregnancy.
• Other protocol-defined exclusion criteria may apply.