Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Szabocsik and Associates, Inc.
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Have been advised that the contact lenses they will be wearing for the next 3 months are being used for investigational purposes and that their informed consent will be needed and documented prior to the start of the study.
Visual acuity must be correctable to 20/30, with spherical lenses ranging in power from -1.00 to -5.00D, astigmatism≤1.50D.
Have been successfully wearing soft (hydrophilic) contact lenses for at least one month prior to entering the study. (Success means both subject and practitioner are satisfied with visual acuity, comfort, and ocular physiology).
Have non-diseased eyes which are normal or which have no preexisting ocular condition which would interfere with the patient's ability to adapt to the new pair of LSH Silicone Hydrogel Soft (hydrophilic) Contact Lenses. A normal eye is defined as one having all the following characteristics:
1. No evidence of lid infection.
2. No structural lid abnormality.
3. No conjunctival abnormality or infection.
4. A cornea which is clear with no edema, staining, vascularization or abnormal opacities, all as observed by slit lamp examination.
5. No iritis.
6. No other active ocular disease that would contraindicate use of the investigational lens.
7. No GPC (giant papillary conjunctivitis, tarsal abnormality) Grade 2 or greater
Use no ocular medication.
Have no known sensitivity to solutions currently used for contact lens care.
Have binocular correction with contact lenses.
You may not be if
Astigmatism \>1.50D
No monocular or monovision fits may be included.
Pregnant and lactating women are excluded from the study
