Dispensing Evaluation of Subjective Comfort, Vision, and Handling of a New Lens Compared to a Marketed Lens

Exclusion Criteria

• •The subject must have no known ocular or systemic allergies that might interfere with contact lens wear.
• •The subject must have no known systemic disease, or need for medication, which might interfere with contact lens wear.
• •The subject's optimal vertexed spherical equivalent distance correction must be between-1.00 and -4.00D.
• •Any cylinder power must be:\<=0.75D.
• •The subject must have visual acuity best correctable to 20/25 or better for each eye.
• •The subject must have normal eyes (no ocular medications or ocular infection of any type).
• •The subject must read and sign the Statement of Informed Consent.
• •The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol.
• •Ocular or systemic allergies or disease which might interfere with contact lens wear.
• •Systemic disease, autoimmune disease, or use of medication which might interfere with contact lens wear.
• •Clinically significant (grade 3 or worse) corneal edema, corneal neovascularization, corneal staining, or any other abnormalities of the cornea which would contraindicate contact lens wear.
• •Clinically significant (grade 3 or 4) tarsal abnormalities or bulbar injection which might interfere with contact lens wear.
• •Any ocular infection.
• •Any corneal distortion resulting from previous hard or rigid gas permeable contact lens wear.
• •Any color deficiencies (color blindness) - to the best of the subject's knowledge.
• •Pregnancy or lactation.
• •Diabetes.
• •Infectious diseases (e.g. hepatitis, tuberculosis) or an immuno-suppressive disease (e.g. HIV).
• •Habitual contact lens type is toric, multifocal, or is worn as extended wear.
• •Subject presents with one dark iris color and one light iris color
• •Subject has heterochromia iridis (a difference in color between parts of one iris)
• •The subject is an employee or family member of the clinical study site.