Status:
COMPLETED
Central Corneal Thickness With SENSIMED Triggerfish
Lead Sponsor:
Sensimed AG
Conditions:
Glaucoma
Ocular Hypertension
Eligibility:
All Genders
18+ years
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.
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
September 1 2010
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
February 1 2011
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT01210963
Start Date
September 1 2010
End Date
February 1 2011
Last Update
March 18 2011
Active Locations (1)
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1
Augen- und Poliklinik, Universitätsklinikum Würzburg
Würzburg, Germany, 97080