Continuous Intraocular Pressure (IOP) Monitoring in Pigmentary Dispersion Syndrome and Pigmentary Glaucoma Patients

Pigmentary Dispersion Syndrome Clinical Trial

Official title: Detection of Induced IOP Fluctuations by SENSIMED Triggerfish® in Pigmentary Syndrome and Glaucoma Patients

Status Terminated

Clinical Trial Summary

This study monitors the intraocular pressure (IOP) over 4 to 6 hours using the SENSIMED Triggerfish® device and Goldmann Applanation Tonometry (GAT) in pigment dispersion syndrome and pigmentary glaucoma patients. The aim of the study is to detect SENSIMED Triggerfish® output signal peak after induced fluctuation by physical exercise or pupil dilation.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Glaucoma
• Glaucoma, Open-Angle
• Pigmentary Dispersion Syndrome
• Pigmentary Glaucoma Patients
• Syndrome

• NCT number: NCT01253109
• Study type: Observational
• Source: Sensimed AG
• Status: Terminated
• Phase: N/A
• Start date: September 2010
• Completion date: November 2011