Clinical Research Directory

Inclusion Criteria: * Adults, ≥40-year-old, CL wearers with best-corrected 20/20 distance visual acuity or better. * Requiring +0.75 ADD or more at standard near distance of 40 cm. * Participants will be required to have worn reusable silicone hydrogel toric CLs in the past year and still at a minimum wearing the CLs occasionally without having significant discomfort or dryness. * All participants will be required to have a CLDEQ-8 score \<12. * Participants will be required to be able to wear Total 30MFT CLs (presbyopic plus astigmatism both ≥0.75D OD and OS). * Astigmatism ranging from 0.75 D to 2.50 D in each eye. * Participants will be required to wear the study CLs for ≥13 hours each day with no overnight wear. * Willing to wear study CLs for ≥16 hours on the Day 1 (1st full day), Day 14, and Day 29 when responses will be collected via text message. * Participants will be willing to wear the CL every day of the week. * Participants will be required to provide a glasses prescription that is less than 3 years old. * Visual acuity with habitual reusable silicone hydrogel toric CLs is 20/25 or better in each eye. Exclusion Criteria: * Have worn Total30 MFT in the past * Are past rigid CL wearers * Are currently wearing monovision CLs * Have a history of being diagnosed with dry eye or ocular allergies * Have known systemic health conditions that are thought to alter tear film physiology * Have a history of viral eye disease * Have a history of ocular surgery * Have a history of severe ocular trauma * Have a history of corneal dystrophies or degenerations * Have active ocular infection or inflammation * Are currently using isotretinoin-derivatives or ocular medications * Are pregnant or breast feeding