The purpose of this study was to confirm the clinical performance of a novel manufacturing process for comfilcon A contact lenses in habitual wearers over a one-month period of lens wear.
This was a prospective, multiple day, double-masked (investigator and subject), randomized, bilateral re-fit parallel arm study comparing a Test Lens against an appropriate Control Lens. Participants were randomized to wear the Test or Control lens for 30±2 days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
77
Daily wear lenses for 30±2 days
Daily wear lenses for 30±2 days
Clinical Research Center, UC Berkeley
Berkeley, California, United States
Clinical Optics Research Lab at IU School of Optometry
Bloomington, Indiana, United States
SUNY College of Optometry Clinical Vision Research Center
New York, New York, United States
Ohio State University College of Optometry
Columbus, Ohio, United States
Visual Acuity
Monocular distance logMAR visual acuity at distance 4 meters under high illumination, high contrast conditions was measured at the 4 week timepoint of lens wear.
Time frame: 4 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
ProCare Vision Center, Inc.
Granville, Ohio, United States