SENSIMED Triggerfish Discomfort During IOP Monitoring

- Patient is able to comply with the study procedure

- Patient is 18-80 years old

- Healthy subject or glaucoma patient

- Patient has consented to be in the trial and signed informed consent is available before any study related procedures are carried out

- Cylinder refraction of no more than +/- 2 diopters in the study eye

- Visual acuity of 20/80 or better in the study eye

- Ability of subject to understand the character and individual consequences of the study

- For women with childbearing potential, adequate contraception

- Subjects wearing contact lenses within the last two years

- Subjects with contraindications for wearing contact lenses

- History of refractive surgery

- History of intraocular surgery in the last three months

- Severe dry eye syndrome

- Keratoconus or other corneal abnormalities

- Conjunctival or intraocular inflammation

- Pregnancy and lactation

- Simultaneous participation in other clinical trials