Tear Film Evaluation of Dailies® AquaComfort Plus® Multifocal and Toric

Inclusion Criteria: * Must sign an informed consent document; * Adapted, current soft contact lens wearer with either: 1. A spectacle add between +0.50 and +2.50 (inclusive) \[Presbyopes group\] 2. A spherical correction of an astigmatism up to 20% of the amount of the sphere \[Astigmats group\]; * Contact lens prescription in the power range specified in the protocol; * Vision correctable to 0.2 logMAR (logarithmic minimal angle for resolution) or better in each eye at distance with pre-study lenses or manifest refraction at Visit 1; * Willing to wear study lenses up to 12 hours and attend all study visits; * Can be successfully fitted with study lenses; * Other protocol-specified inclusion criteria may apply. Exclusion Criteria: * Any ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear; * Use of systemic or ocular medications for which contact lens wear could be contraindicated as determined by the investigator; * Use of artificial tears and rewetting drops during the study; * Monocular (only 1 eye with functional vision) or fit with only 1 lens; * Any abnormal ocular condition observed during the Visit 1 slit-lamp examination; * History of herpetic keratitis, ocular surgery, or irregular cornea; * Pregnant or lactating; * Unstable tear film with a NIK-BUT value below 8 seconds in either eye without lenses; * Participation in any clinical study within 30 days of Visit 1; * Other protocol-specified exclusion criteria may apply.