Clinical Trials Directory

Trials / Completed

CompletedNCT01217853

24h Continuous Intraocular Pressure (IOP) Monitoring vs Goldmann Applanation Tonometry

Comparison of 24-hour Continuous IOP Monitoring With a Contact Lens-based Sensor to Goldmann Applanation Tonometry

Status
Completed
Phase
Study type
Observational
Enrollment
30 (estimated)
Sponsor
Sensimed AG · Industry
Sex
All
Age
40 Years – 70 Years
Healthy volunteers
Not accepted

Summary

A study in which intraocular pressure (IOP) will be monitored over 24 hours using the SENSIMED Triggerfish® device and Goldmann applanation tonometry (GAT) in primary open angle glaucoma patients. The aim of this study is to investigate the comparability of diurnal IOP patterns emerging from SENSIMED Triggerfish and GAT.

Conditions

Interventions

TypeNameDescription
DEVICESENSIMED TriggerfishContact lens-based device for continuous intraocular pressure monitoring

Timeline

Start date
2010-08-01
Primary completion
2011-06-01
Completion
2011-08-01
First posted
2010-10-08
Last updated
2011-08-03

Locations

2 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT01217853. Inclusion in this directory is not an endorsement.

24h Continuous Intraocular Pressure (IOP) Monitoring vs Goldmann Applanation Tonometry (NCT01217853) · Clinical Trials Directory