Glaucoma, Ocular Hypertension
Conditions
Brief summary
Investigation of the occurrence of possible corneal swelling after continuous Intraocular pressure (IOP) monitoring with a contact lens-based Sensor during the sleeping period.
Interventions
DEVICESENSIMED Triggerfish
Contact lens-based Sensor with recording system for continuous monitoring of IOP fluctuation
Sponsors
Sensimed AG
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* glaucoma and ocular hypertension scheduled for overnight hospitalisation * stable IOP-lowering treatment since at least 4 weeks before study * at least 18 years * having provided informed consent
Exclusion criteria
* contact lens wear within the last 2 years * contraindication for silicone lean wear * corneal abnormality in either eye * ocular infection or inflammation * history of ocular surgery within the last 3 months * full-frame metal glasses during IOP monitoring with SENSIMED Triggerfish * pregnancy and lactation * patients not able to understand the nature of the research * patients under tutelage * patients committed to an institution by virtue of an order issued either by the courts or by an authority * simultaneous participation in other clinical research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pachymetry (central corneal thickness) | after 8 hours nocturnal continuous IOP monitoring |
Countries
Germany
Outcome results
None listed