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Study identifier: NCT07586982 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Clinical Performance of Verofilcon A Toric Contact Lenses

Condition: Contact Lenses · Presbyopia  ·  Sponsor: Southern College of Optometry

PhaseNA
Planned participants32
Who can joinAll sexes, 18 Years to 40 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to \[primary purpose: is to determine if Total30 Multi focal toric conntact lensesare comfortable and the willigness for those who have previously worn reusable toric contact lenses are willing to stay in Total30 MFT after 1 month of wear during the duration of the study. Healthy previous reusable toric contact lens weareres will be refit into total30 MFT contact lenses and will be asked to gauge their comfort while wearing the lenses. Healthy adult participants who are presybyopic between the ages of 18-40 can participant, sex and gender are not disqualifiers unless the participant is pregnant or breast feeding. The main question\[s\] it aims to answer \[is/are\] \[primary hypothesis or outcome measure 1Proportions of toric CL wearers who have positive visual acuity scores in comfort and vision after one month of wear. \[primary hypothesis or outcome measure 2\]? Contact lens dry eye-8 scores will be less than 12 indicating high levels of comfort after one month of wear.

This description comes directly from the study's public registry record.

Talk to the study team

Chris Lievens, OD  ·  (901) 722-3200  ·  clievens@sco.edu

Always discuss trial participation with your own doctor first.

Locations (1)

The Southern College of OptometryMemphis, Tennessee, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07586982