Clinical Trials Directory

Trials / Terminated

TerminatedNCT01253109

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

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

Status
Terminated
Phase
Study type
Observational
Enrollment
15 (estimated)
Sponsor
Sensimed AG · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICESENSIMED TriggerfishContact lens-based device for continuous IOP monitoring

Timeline

Start date
2010-09-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2010-12-03
Last updated
2012-01-24

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT01253109. Inclusion in this directory is not an endorsement.

Continuous Intraocular Pressure (IOP) Monitoring in Pigmentary Dispersion Syndrome and Pigmentary Glaucoma Patients (NCT01253109) · Clinical Trials Directory