| Eligibility |
Inclusion Criteria:
1. Is of legal age (at least 18) on the date the Informed Consent Form (ICF) is signed
2. Is able to read, understand, and provide written informed consent on the Institutional
Review Board (IRB)/Ethics Committee (EC) approved ICF and provide authorization as
appropriate for local privacy regulations
3. Is a habitual wearer (at least 3 months)
4. Has typically cleaned and disinfected their pre-study contact lenses daily
5. Must have spectacle correctable distance visual acuity through spherocylindrical
refraction to 40 letters (0.14 logarithm of the minimal angle of resolution (logMAR)
or better in each eye, at 2 meters distance with high contrast chart
6. Has clear central corneas and is free of any anterior segment disorders
7. Is a habitual user of a lens care product for cleaning, disinfecting, and storage of
lenses
8. Requires lens correction in both eyes
9. Wears the same manufacturer and brand of lens in both eyes
10. Agrees to wear study lenses on a daily wear basis for approximately three months
11. Is willing and able to comply with all treatment and follow-up/study procedures.
Exclusion Criteria:
1. Is currently using a hydrogen-peroxide cleaning and disinfecting solution
2. Participated in any drug or device clinical investigation within 30 days prior to
entry into this study
3. Is a female of childbearing potential (those who are not surgically sterilized or
postmenopausal) if they meet any one of the following conditions:
- they are currently pregnant
- they plan to become pregnant during the study
- they are breastfeeding
4. Has worn gas permeable (GP) lenses within the last 30 days
5. Has worn polymethylmethacrylate (PMMA) lenses within the last three months
6. Has typically worn their pre-study contact lenses on an extended wear basis, sleeping
in their lenses one night or more per week, during the last year
7. Has any systemic disease currently affecting ocular health or which in the
Investigator's opinion may have an effect on ocular health during the course of the
study
8. Subjects with an active ocular disease, or who are using any ocular medication.
9. Is using any medications that will, in the Investigator's opinion, affect ocular
physiology or lens performance
10. Currently wears monovision, multifocal, or toric contact lenses
11. Has ocular astigmatism of 1.00D or greater in either eye
12. Has anisometropia (spherical equivalent) of greater than 2.00D
13. Has any grade 2 or greater finding during the slit-lamp examination (refer to Appendix
B for Methods of Clinical Evaluation)
14. Has corneal infiltrates, of ANY GRADE
15. Has any "Present" ungraded finding during the slit-lamp examination (refer to Appendix
B for Methods of Clinical Evaluation) that, in the Investigator's judgment, interferes
with contact lens wear.
16. Has typically worn their pr-study control lenses on an extended wear bases, sleeping
on their lenses one night or more per week, during the last year.
17. Is aphakic
18. Is amblyopic
19. Has had any corneal surgery (e.g., refractive surgery)
20. Is allergic to any component in the study care products.
21. Is an employee of any of the study investigative sites or a family member of an
employee of the investigative site, including family members living outside of the
employee's household
22. Is an Ophthalmologist, an Optometrist, an Optician, or an Ophthalmic
Assistant/Technician, or currently resides with a person with any of these specialties
23. Is an employee of a manufacturer of contact lenses or contact lens care products
(e.g., Alcon, Bausch + Lomb, Ciba Vision, CooperVision, Vistakon, Johnson & Johnson,
etc.) or currently resides with a person employed by any of these manufacturers.
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