The purpose of this clinical trial is to assess the clinical performance of LID223194 Multifocal (MF) contact lenses and commercially available Air Optix plus HydraGlyde (AOHG) MF contact lenses. Eligible subjects will wear each study lens type in a cross-over fashion as randomized for approximately 2 days.
Subjects will be expected to attend 3 scheduled visits for an individual duration of participation of up to 10 days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
16
Silicone hydrogel multifocal contact lenses
Silicone hydrogel multifocal contact lenses
Commercially available cleaning and disinfection system for silicone hydrogel contact lenses
Johns Creek Research Clinic
Johns Creek, Georgia, United States
Mean Binocular Visual Acuity (VA) With Study Lenses at 4 Meters (logMAR)
VA was assessed binocularly (both eyes together) using a letter chart and measured in logarithm minimum angle of resolution (logMAR). A logMAR value of 0 equates to 20/20 Snellen visual acuity (normal distance eyesight), with lower logMAR values indicating better visual acuity. No hypothesis testing was pre-specified for this endpoint.
Time frame: Day 2 of each study lens type worn during the corresponding crossover period
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