Use of an Ocular Telemetry Sensor in Tafluprost Treated Patients

Status Terminated

Clinical Trial Summary

This clinical trial is designed to investigate the performance of SENSIMED Triggerfish® during 24-hour continuous IOP fluctuation monitoring, defined as the number of valid recording intervals over the 24-hour period.

The investigation will recruit male and female patients older than 18 years and diagnosed with glaucoma and treated with tafluprost in both eyes. 20 subjects will be enrolled in the study. Patients will be considered enrolled in the study upon signature of informed consent. A screening visit and one 24-hour IOP fluctuation monitoring session during a 36-hour hospitalisation, are planned for each patient.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Glaucoma

Clinical Trial Details

NCT number	NCT01263535
Study type	Interventional
Source	Sensimed AG
Contact
Status	Terminated
Phase	Phase 4
Start date	September 2010
Completion date	May 2012

View Details

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