Clinical Research Directory

Inclusion Criteria: Subjects are eligible for the study if they meet the following criteria: * Subjects who currently wear soft multi-focal contact lenses and score \<12 on an entering CLDEQ-8 survey. * Subjects who are \>= 40 years old. * Subjects who can and are willing to wear their lenses for 13 hours per day during the study period, and 16 hours per day when questionnaires are being taken. * Willing to insert their contact lenses between 6:00 am and 8:00 am on the days when questionnaires will be taken. * Vision correctable in soft multi-focal contact lenses to 20/25 (0.10 log MAR) or better in each eye at 6M. * Must be able to be successfully fit into the prescription parameters available for Total30 MF contact lenses. * Required to have a smartphone and receive push notifications. * Willing to attend all study visits. * Willing to be diligent about answering the timed surveys in a prompt manner. Exclusion Criteria: If any of the following exclusion criteria are applicable, the subject should not be enrolled in the study. * 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 isotretinoin-derivatives. * Use of lubricating drops. * Monocular patients or patients fit with only 1 multifocal lens. * Prior refractive surgery. * History of herpetic keratitis, ocular surgery, or irregular cornea. * Pregnant or lactating. * Having participated in a clinical trial in the past 30 days. * High-ADD habitual wearers using a different fitting approach than Alcon's multifocal fitting guide (e.g., J\&J or CooperVision's fitting guide adopting a modified monovision approach). * Are past rigid CL wearers. * Have a history of being diagnosed with dry eye or ocular allergies. * Have history of severe ocular trauma.