Clinical Characterization of Symptomatic Populations

Exclusion Criteria

• •Potential subjects who meet any of the following criteria will be excluded from participating in the study:
• •1. Currently pregnant or lactating, by self-report.
• •2. Any ocular or systemic allergies, disease or use of medication which may interfere with contact lens wear (at the discretion of the investigator).
• •3. Any active ocular abnormalities/conditions that may interfere with contact lens wear (at the discretion of the investigator).
• •4. Any infectious diseases (e.g. hepatitis, tuberculosis) or a contagious immunosuppressive disease (e.g. HIV), by self-report.
• •5. Any corneal distortion resulting from previous hard or rigid gas permeable contact lens wear.
• •6. Habitual contact lens wear modality as extended wear (≥1 night per month of extended wear).
• •7. Habitual contact lens is rigid gas permeable, toric, monovision or multi-focal
• •8. Any previous, or planned (during the course of the study) ocular surgery (e.g., radial keratotomy, PRK, LASIK, etc.)
• •9. Participation in any contact lens or lens care product clinical trial within 2 weeks prior to study enrollment.
• •10. Employee or employee's immediate family member of clinical site (e.g., Investigator, Coordinator, Technician).
• •11. Current habitual use of Restasis, Xiidra, ocular steroids, or any medication (RX or OTC) that may interfere with contact lens wear (at the discretion of the investigator).