Central Corneal Thickness With SENSIMED Triggerfish

Sensimed AG20 enrolled

Overview

Investigation of the occurrence of possible corneal swelling after continuous Intraocular pressure (IOP) monitoring with a contact lens-based Sensor during the sleeping period.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Glaucoma Ocular Hypertension

Interventions

SENSIMED TriggerfishDEVICE

Contact lens-based Sensor with recording system for continuous monitoring of IOP fluctuation

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Augen- und Poliklinik, Universitätsklinikum Würzburg

Würzburg, Germany

Outcomes

Primary Outcomes

Pachymetry (central corneal thickness)

Time frame: after 8 hours nocturnal continuous IOP monitoring

Data from ClinicalTrials.gov

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