Clinical Evaluation Of Two Daily Disposable Contact Lenses And A Monthly Replacement Lens

Inclusion Criteria:

- Be no less than 18 and no more than 39 years of age.

- Sign Written Informed Consent and investigator to record this on Case Report Form (See
separate document).

- Be willing and able to adhere to the instructions set out in the protocol.

- Own a cell phone and be willing to receive text messages during the day.

- Be an existing successful daily wear soft contact lens. For the purposes of this study
this means wearing lenses for at least 6 hours per day, 5 days per week for the last
month.

- No extended wear in the last 3 months.

- Subjective refraction must result in a vertexed spherical contact lens prescription
between -1.00 and -6.00D.

- Have refractive astigmatism less than or equal to 1.00D in both eyes.

- Achieve visual acuity of 6/9 (20/30) or better in each eye.

- Require a visual correction in both eyes (no monofit or monovision allowed).

- Does not require presbyopic correction (i.e. Not using any presbyopic correction and
measured add power of less than +1.00D).

- Have normal eyes with no evidence of abnormality or disease. For the purposes of this
study a normal eye is defined as one having:

- No amblyopia.

- No evidence of lid abnormality or infection (including blepharitis/meibomitis).

- No conjunctival abnormality or infection.

- No clinically significant slit lamp findings (i.e. stromal edema,
vascularization, infiltrates or abnormal opacities).

- No other active ocular disease.

Exclusion Criteria:

- Requires concurrent ocular medication.

- Clinically significant (Grade 3 or 4) corneal stromal haze, corneal vascularization,
tarsal abnormalities, bulbar hyperemia, limbal hyperemia, or any other abnormality of
the cornea that would contraindicate contact lens wear.

- Clinically significant corneal staining (Grade 3 in more than one corneal region per
eye).

- Requires presbyopic correction (i.e. Not using any presbyopic correction and measured
add power of less than +1.00D).

- Has had refractive surgery.

- Has had eye injury/surgery within 8 weeks immediately prior to enrolment for this
study.

- Abnormal lacrimal secretions.

- Pre-existing ocular irritation that would preclude contact lens fitting.

- Keratoconus or other corneal irregularity.

- PMMA(polymethyl methacrylate), hybrid or RGP(rigid gas permeable) lens wear in the
previous 8 weeks.

Does not require presbyopic correction (i.e. Not using any presbyopic correction and
measured add power of less than +1.00D).

- Any systemic illness which would contraindicate lens wear or the medical treatment of
which would affect vision or successful lens wear.

- Diabetic.

- Infectious disease (e.g., hepatitis, tuberculosis) or an immunosuppressive disease
(e.g., HIV (Human immunodeficiency virus)).

- History of chronic eye disease (e.g. glaucoma or ARMD (age related macular
degeneration)).

- Pregnancy, lactating or planning a pregnancy at the time of enrolment.

- Participation in any concurrent clinical trial or in last 30 days.