Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Johnson & Johnson Vision Care, Inc.
Age
35–70
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
The subject must between 35 and 70 years of age.
The subject must have presbyopic symptoms or be already wearing presbyopic contact lens correction.
The subject's spherical equivalent distance refraction must be in the range of -1.00 to -6.00 or -9.00 to -10.00 in each eye.
Refractive cylinder must be -0.75 D in each eye.
The subject must have an ADD power of +0.75D to +2.50D in each eye.
The subject must have best corrected visual acuity of 20/20-3 or better in each eye
The subject's must have at least 20/30-distance vision OU with the study contact lenses.
The subject must agree that they are comfortable with their vision prior to being dispensed the study lenses
The subject must be an adapted soft contact lens wearer in both eyes.
The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol.
The subject must read and sign the STATEMENT OF INFORMED CONSENT and be provided a copy of the form.
You may not be if
Ocular or systemic allergies or disease that may interfere with contact lens wear.
Systemic disease, autoimmune disease or use of medication, which may interfere with contact lens wear.
Clinically significant (grade 3 or 4) corneal edema, corneal vascularization, corneal staining or any other abnormality of the cornea, which may contraindicate contact lens wear
Clinically significant (grade 3 or 4) tarsal abnormalities that might interfere with contact lens wear.
Any ocular infection.
Any corneal distortion resulting from previous hard or rigid gas permeable contact lens wear.
Pregnancy or lactation
Any infectious disease (e.g., hepatitis, tuberculosis) or an immunosuppressive disease (e.g., HIV).
History of diabetes
History of binocular vision abnormality or strabismus
