The purpose of this study is to investigate the overall clinical performance of the somofilcon A daily disposable test soft contact lens compared to the somofilcon A daily disposable control soft contact lens.
The purpose of this study is to evaluate the clinical performance of an investigational silicone-hydrogel contact lens (test) against a marketed silicone-hydrogel contact lens (control) when worn on a daily disposable wear modality over 1 week (for each lens) in a randomized, bilateral, cross-over, dispensing study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
36
Contact lens
Contact lens
Center for Contact Lens Research, University of Waterloo
Waterloo, Ontario, Canada
Comfort
Subjective comfort scored 0-100 (0=Cannot be worn, 100=Cannot be felt ever)
Time frame: up to 1 week
Preference
Overall lens that subject prefers or no preference
Time frame: up to 1 week
Vision
Visual acuity measured in logMAR
Time frame: Up to 1 week
Subjective Vision
Subjective vision scored 0-100 (0=Extremely poor, 100=Excellent vision all the time)
Time frame: up to 1 week
Corneal Staining
Amount of staining observed on the cornea scored 0-4 (0=none, 4=severe) in 0.25 steps
Time frame: up to 1 week
Conjunctival Staining
Amount of staining observed on the conjunctiva scored 0-4 (0=none, 4=severe) in 0.25 steps
Time frame: up to 1 week
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