Clinical Validation of iCare IC1000 Tonometer

Exclusion Criteria

• •Subjects with only one functional eye
• •Subjects having poor or eccentric fixation in the study eye
• •High corneal astigmatism \>3D in the study eye
• •Central corneal scarring
• •History of prior incisional glaucoma surgery or corneal surgery, including corneal refractive laser surgery in the study eye
• •Microphthalmos
• •Buphthalmos
• •Contact lens use within one week of continuous wear and within one hour if lens is worn occasionally
• •Dry eyes (clinically significant)
• •Lid squeezers - blepharospasm
• •Nystagmus
• •Keratoconus
• •Any other corneal or conjunctival pathology or infection relevant to this study
• •Central corneal thickness greater than 600 µm or less than 500 µm in the study eye
• •Cataract Extraction within last 2 months in the study eye