A subject with any UNCONTROLLED systemic disease.A subject whose best-corrected visual acuity is worse than 20/40 in their surgical eye.Contact lens usage within 6 months for PMMA contacts lenses, 1 month for gas permeable lenses or 1 week for extended-wear and daily-wear soft contact lenses.Pupil abnormalities (non-reactive, tonic pupils, abnormally shaped pupils, or pupils that do not dilate at least 4.0 mm under mesopic/scotopic conditions).Capsule or zonular abnormalities that may affect postoperative centration or tilt of the lens (e.g.Subjects who may be expected to require retinal laser treatment or other surgical intervention.macular degeneration, or other retinal disorders) that are predicted to cause future acuity losses to a level of 20/30 or worse Diagnosed degenerative visual disorders (e.g.Known pathology that may affect visual acuity particularly retinal changes that affect vision (macular degeneration, cystoid macular edema, proliferative diabetic retinopathy, etc.).History of ocular trauma or prior ocular surgery.intracanalicular plug(s) or a history of punctual cautery in the study eye. Remembering to blink more often can help keep the eye surface wet. Uncontrolled systemic or ocular disease To evaluate the safety and efficacy of BLINK tears compared with NO topical. In some cases, permanent closure with surgical cautery may be used.diabetes mellitus, immunocompromised, etc.) Acute or chronic disease or illness that would increase risk or confound study results (e.g.Use of systemic or ocular medications that may affect vision.Likely to complete the entire course of the study.Patients not currently using any artificial tears regularly, or using low viscosity tears for symptom relief (Refresh Tears, Visine Tears, Tears Naturelle, etc.).Has undergone cataract surgery in only one eye and has received a Tecnis multi-focal intraocular lens in the study eye.Has 20/40 or better best corrected visual acuity in the surgical eye at the Day 1 post-op visit (Visit 3).Written, informed consent and HIPPA Authorization.Male or female subjects, 21 years of age or older.Why Should I Register and Submit Results?.
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