Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Sensimed AG
Age
18–80
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject is able to comply with the study procedures
Subject is 18-80 years old
Glaucoma patient, with glaucomatous optic neuropathy based on clinical assessment of stereoscopic optic disc photographs and/or repeatable abnormal standard automated perimetry (SAP) visual fields at baseline, defined as a pattern standard deviation with P\<0.05 or a glaucoma Hemifield test "outside normal limits
Glaucoma suspect, with suspicious optic disc appearance (as determined by subjective assessment on the baseline visit) or elevated IOP (\>21 mmHg) but normal and reliable SAP visual fields at baseline
Subject has consented to be in the trial and signed informed consent is available before any study related procedures are carried out
Visual acuity of 20/200 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
You may not be if
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, except prior uncomplicated cataract surgery a minimum of 3 months prior to the investigation
Full frame metal glasses during SENSIMED Triggerfish® recording
Known hypersensitivity to silicone, plaster or ocular anesthesia
Pregnancy and lactation
Simultaneous participation in other clinical studies
Clareo Health | SENSIMED Triggerfish Safety and Tolerability
