Central Corneal Thickness With SENSIMED Triggerfish
Completed
- Conditions
- GlaucomaOcular Hypertension
- Interventions
- Device: SENSIMED Triggerfish
- Registration Number
- NCT01210963
- Lead Sponsor
- Sensimed AG
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description SENSIMED Triggerfish SENSIMED Triggerfish -
- Primary Outcome Measures
Name Time Method Pachymetry (central corneal thickness) after 8 hours nocturnal continuous IOP monitoring
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Augen- und Poliklinik, Universitätsklinikum Würzburg
🇩🇪Würzburg, Germany