The aim of this study is to assess contact lens performance and acceptance.
The objective of this study is to assess the initial performance and acceptance of a range of contact lenses in habitual soft contact lens wearers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
250
Participants will be randomized to wear somofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear stenfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear fanfilcon A soft contact lens for 10 hours.
Indiana University
Bloomington, Indiana, United States
RECRUITINGHigh contrast, high luminance binocular distance visual acuity
High contrast, high luminance binocular distance visual acuity (logMAR) will be measured at 10-hour visit.
Time frame: At the end of 10 hours of daily wear at dispensing
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Participants will be randomized to wear comfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear verofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear serafilcon A soft contact lens for 10 hours.
Participants will be randomized to wear lehfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear delefilcon A soft contact lens for 10 hours.
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear senofilcon A soft contact lens for 10 hours.
Participants will be randomized to wear samfilcon A soft contact lens for 10 hours.
Participants will be randomized to wear kalifilcon A soft contact lens for 10 hours.