24-hr Intraocular Pressure (IOP) Patterns of Glaucoma Patients After Selective Laser Trabeculoplasty (SLT)

Inclusion Criteria:

- Subjects must correspond to all other inclusion criteria in order to be eligible for
the investigation.

- Subject is able to comply with the study procedures

- 18-80 years old

- Subjects diagnosed with glaucoma, based on presence of repeatable visual field
loss and/or glaucomatous optic neuropathy based on masked review of optic disc
stereophotographs and under ocular hypotensive treatment, or diagnosed with
ocular hypertension, with an IOP of > 22 mmHg at the screening visit and under
ocular hypotensive treatment.

- Subject has consented to be in the trial

- Visual acuity of 20/200 or better

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

- For women of childbearing potential, adequate contraception

Exclusion Criteria:

- Subjects presenting with any of the following criteria will not be included in the
trial:

- Subjects with contraindications for wearing contact lenses

- Severe dry eye syndrome

- Keratoconus or other corneal abnormality

- Conjunctival or intraocular inflammation

- Eye surgery prior to and throughout the study.

- Full frame metal glasses during SENSIMED Triggerfish® monitoring

- Known hypersensitivity to silicone, plaster or ocular anesthesia (proparacaine)

- Pregnancy and lactation

- Simultaneous participation in other clinical studies