Evaluation of ACUVUE® OASYS 1-Day for Astigmatism Contact Lenses With Alternative Lidstock

Exclusion Criteria

• •Potential subjects who meet any of the following criteria will be excluded from participating in the study:
• •The subject must not:
• •1. Be currently pregnant or lactating.
• •2. Be diabetic.
• •3. Be currently using any ocular medications or have an ocular infection of any type.
• •4. Have any ocular or systemic allergies, disease, infection, or use of medication that might contraindicate or interfere with contact lens wear or otherwise compromise study endpoints, including infectious diseases (e.g., hepatitis, tuberculosis), contagious immunosuppressive disease (e.g., Human Immunodeficiency Virus \[HIV\]), or history of serious mental illness or seizures. See section 9.1 for additional details regarding systemic medications.
• •5. Have habitually worn rigid gas permeable (RGP) lenses, orthokeratology lenses, or hybrid lenses (e.g., SynergEyes, SoftPerm) within the past 6 months.
• •6. Be currently wearing monovision or multifocal contact lenses or be currently wearing lenses in an extended wear modality.
• •7. Have a history of strabismus or amblyopia.
• •8. Be an employee (e.g., Investigator, Coordinator, Technician) or family member of an employee of investigational clinic.
• •9. Have participated in a contact lens or lens care product clinical trial within 7 days prior to study enrollment.
• •10. Have clinically significant (Grade 3 or 4 on the FDA classification scale) slit lamp findings (e.g., corneal edema, neovascularization or staining, tarsal abnormalities or bulbar injection) or other corneal or ocular disease or abnormalities that may contraindicate contact lens wear or otherwise compromise study endpoints (including entropion, ectropion, chalazia, recurrent styes, glaucoma, history of recurrent corneal erosions, aphakia, moderate or above corneal distortion, herpetic keratitis).
• •11. Have fluctuations in vision due to clinically significant dry eye or other ocular conditions.
• •12. Have had or have planned (within the study period) ocular or intraocular surgery (e.g., radial keratotomy, PRK, LASIK, etc.).