Central Corneal Thickness With SENSIMED Triggerfish

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

Completed

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Key information

Conditions

Glaucoma Eye Diseases Ocular Hypertension

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Augen- und Poliklinik, Universitätsklinikum Würzburg

Würzburg, 97080, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

SENSIMED Triggerfish

Device

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

Primary outcomes

Pachymetry (central corneal thickness)

Time frame: after 8 hours nocturnal continuous IOP monitoring

Sponsors and collaborators

Lead sponsor

Sensimed AG

Industry

Registry information

Official study title

Central Corneal Thickness After Overnight IOP Monitoring With SENSIMED Triggerfish

Acronym: 09/08

Important dates

Study start: 2010
Primary completion: 2011
Study completion: 2011
First posted: Sep 29, 2010
Registry last updated: Mar 18, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed