Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 2

Launched by ALCON RESEARCH · Aug 24, 2020

Keywords

ClinConnect Summary

Subjects are expected to attend 3 study visits and wear the PRECISION1 and Clariti 1-Day study lenses in a crossover design for approximately 8 days of exposure to each study lens type. The expected duration of subject participation is up to 22 days.

Gender

ALL

Eligibility criteria

• • Key Inclusion Criteria
• • Subject must be able to understand and must sign an Institution Review Board (IRB) approved Informed Consent Form.
• • Successful wear of soft contact lenses in both eyes for a minimum of 5 days per week and 10 hours per day during the past 3 months.
• • Willing to wear contact lenses for at least 16 hours per day on one of the days with each lens type.
• • Other protocol-specified inclusion criteria may apply.
• Key Exclusion Criteria:
• • Any ocular condition that contraindicates contact lens wear.
• • Previous or current habitual wearer of PRECISION1, Clariti 1-Day, or DAILIES TOTAL1 contact lenses.
• • Other protocol-specified exclusion criteria may apply.