Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
CooperVision, Inc.
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Informed Consent and HIPAA document read, signed, and dated.
Visual acuity correctable to 20/30 (Snellen) or better in each eye at distance with hydrogel or silicone hydrogel contact lenses.
Successfully wearing hydrogel or silicone hydrogel contact lenses on a daily wear basis for at least two weeks prior to the study.
You may not be if
History of hypersensitivity
Evidence or history of epithelial herpes simplex keratitis (dendritic keratitis; vaccinia, active or recent varicella, viral disease of the cornea and/or conjunctiva and/or eyelids; bacterial infection of the eye; and/or fungal disease of the eye
One functional eye or a monofit eye
Ocular conditions such as active acute blepharitis, conjunctival infections, and iritis
Type 2 (macropunctate) or greater corneal staining in any region in either eye as observed by slit-lamp at Visit 1 of each study period
Sum of the type of corneal staining greater than or equal to 4 across entire cornea in either eye as observed by slit-lamp at Visit 1 of each study period
Conjunctival staining covering greater than or equal to 20% in 2 or more corneal regions in either eye as observed by slit-lamp at Visit 1 of each study period
Conjunctival injection greater than Grade 2 (moderate-diffuse redness) in either eye as observed by slit-lamp at Visit 1 of each study period
Abnormal lenticular opacity in the visual axis of the lens in either eye
Use of concomitant topical Rx or over-the-counter (OTC) ocular medications
History of seasonal allergies with significant ocular side effects which may have an adverse impact on contact lens wear
Pregnant or lactating females
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