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

Inclusion Criteria:

- Must sign an informed consent document;

- Adapted, current soft contact lens wearer;

- Contact lens prescription in the power range specified in the protocol;

- Vision correctable to 0.2 (logMAR) 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.