DAILIES TOTAL1® Lens Centration in a Japanese Population

Inclusion Criteria: * Sign Informed Consent document. * Habitually wear soft contact lenses on a daily disposable or weekly/monthly replacement basis. * Symptoms of contact lens discomfort as defined by protocol. * Require contact lenses within the power range of -0.50 diopter (D) to -10.00 D. * Cylinder, if present, less or equal to 0.75D in either eyes at Visit 1. * Vision correctable to 20/25 or 0.1 (logMAR) or better in each eye at distance with pre-study lenses at Visit 1. * Acceptable contact lens fit with both study contact lenses. * Willing to wear lenses every day for at least for a minimum of five days per week six hours per day, every day if possible and attend all study visits. * Other protocol-defined inclusion criteria may apply. Exclusion Criteria: * Currently wearing DT1 or 1DAVTE. * Ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear. * Use of systemic or ocular medications which contact lens wear could be contraindicated as determined by the investigator. * Eye injury or surgery within twelve weeks immediately prior to enrollment for this trial. * Any moderate or severe ocular condition observed during the slit-lamp examination at the enrollment visit. * History of herpetic keratitis, ocular surgery or irregular cornea. * Prior refractive surgery (e.g. LASIK, PRK, etc). * Monocular subjects (only one eye with functional vision) or subjects fit with only one lens. * Judged ineligible as a patient in this clinical study by the investigator. * Other protocol-defined exclusion criteria may apply.