Comparison of Two Daily Disposable Contact Lenses Over 1-week of Wear

Inclusion Criteria

• •The subject must be between 18 and 45 years of age (inclusive) with no presbyopic add.
• •The subject must read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form. This should be recorded on the Case Report Form (CRF).
• •The subject must be willing to wear the study lenses for at least 8 hours per day, 7 days per week.
• •The subject must be a current successful soft contact lens wearer in both eyes
• •The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol.
• •The subject's subjective refraction must result in a vertex corrected spherical contact lens prescription in the range of -1.00D to -6.00D in each eye.
• •The subject's refractive astigmatism must be less than or equal to 0.75D in both eyes.
• •The subject must have best corrected visual acuity of 20/30 (6/9) or better in each eye.
• •The subject must require a visual correction in both eyes (no monofit or monovision allowed).
• •The subject must have normal eyes with no evidence of abnormality or disease. For the purposes of this study a normal eye is defined as one having:
• •1. No amblyopia.
• •2. No evidence of lid abnormality or infection (including blepharitis/meibomitis).
• •3. No conjunctival abnormality or infection.
• •4. No clinically significant slit lamp findings (i.e. stromal edema, vascularization, infiltrates or abnormal opacities).
• •5. No other active ocular disease.