The purpose of this study is to assess the clinical performance of two reusable silicone hydrogel contact lenses when worn on a daily wear basis.
In this crossover study, subjects will wear each study lens type for approximately 14 days and attend 7 scheduled visits. The expected duration of subject participation in the study is approximately 28 days (approximately 14 days per each study lens type).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
68
Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection
Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection
Hydrogen peroxide based contact lens cleaning and disinfecting solution
Drs. Giedd, PA
Maitland, Florida, United States
Wesley Optometric Consulting
Medina, Minnesota, United States
ProCare Vision Center
Granville, Ohio, United States
West Bay Eye Associates
Warwick, Rhode Island, United States
Visual Acuity With Study Lenses at Week 1 Follow-Up
Visual acuity (VA) was assessed with study lenses in place using logarithmic of the Minimum Angle of Resolution (logMAR) charts. A logMAR acuity of 0.0 corresponds to 20/20 Snellen acuity (normal visual acuity), with a negative value denoting better than 20/20 visual acuity. Each eye was assessed individually. No hypothesis testing was pre-specified for this endpoint.
Time frame: Week 1, each wear period. A wear period was approximately 14 days.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Optometry Group, PLLC
Memphis, Tennessee, United States