Evaluation of Comfilcon A and Senofilcon A Lenses
Non-dispensing, single-masked, randomized, contralateral study comparing the test lens against the control lens. Each subject will be randomized to wear the test lens in one eye and the control lens in the other eye.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
61
Senofilcon A; Comfilcon A
Comfilcon A; Senofilcon A
University of Houston College of Optometry, TERTC
Houston, Texas, United States
Subjective Responses for Comfort Rated on a 0-100 Visual Scale.
Subjective Patient Ratings measured using a Visual Analog Scale on a 0-100. (0=Cannot be worn. Causes pain, 20=Frequently irritating, 40=Occasionally irritating, 60=Occasionally noticeable but not irritating, 80=Rarely noticeable, 100=Cannot be felt ever)
Time frame: Baseline Insertion, 10 Minutes, 5 hours and 10 hours
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