Clinical Trials Directory

Trials / Completed

CompletedNCT01210963

Central Corneal Thickness With SENSIMED Triggerfish

Central Corneal Thickness After Overnight IOP Monitoring With SENSIMED Triggerfish

Status
Completed
Phase
Study type
Observational
Enrollment
20 (estimated)
Sponsor
Sensimed AG · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DEVICESENSIMED TriggerfishContact lens-based Sensor with recording system for continuous monitoring of IOP fluctuation

Timeline

Start date
2010-09-01
Primary completion
2011-02-01
Completion
2011-02-01
First posted
2010-09-29
Last updated
2011-03-18

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01210963. Inclusion in this directory is not an endorsement.