|   NearVision CK should not be used in patients 
              with the following characteristics:  
              • Peripheral pachymetry reading < 560 µm (measured 
                at the 6 mm optical zone)
 • Strabismus surgery or are likely to develop strabismus 
                following the Conductive Keratoplasty procedure
 
 • Anterior segment pathology, including a cataract, in the 
                eye to be treated
 
 • Any corneal abnormality, such as recurrent corneal erosion 
                or severe basement membrane disease, in the eye to be treated
 
 • Ophthalmoscopic signs of progressive or unstable hyperopia 
                in the eye to be treated
 
 • Distorted or unclear central keratometry corneal mires 
                in the eye to be treated
 
 • Blindness in the fellow eye(one eyed patient)
 
 • Previous intraocular or corneal surgery, including any 
                refractive or therapeutic surgery, in the eye to be treated
 
 • History of herpes zoster or herpes simplex keratitis
 
 • History of steroid-responsive rise in intraocular pressure, 
                glaucoma, or have a preoperative IOP >21 mm Hg
 
 • Risks for angle-closure or have a potentially occludable 
                angle
 
 • Diabetes, diagnosed autoimmune disease, connective tissue 
                disease or clinically significant atopic syndrome
 
 • Current treatment with chronic systemic corticosteroid 
                or other immunosuppressive therapy that may affect wound healing, 
                and any immunocompromised patients
 
 • Using ophthalmic medications, other than artificial tears, 
                for treatment of any ocular disease
 
 • Using systemic medications with significant ocular side 
                effects
 
 • History of keloid fomation
 
 • History or current case of intractable keratoconjunctivitis 
                sicca
 
 • Pregnant, lactating or plan to become pregnant
 
 
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