Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01906151

IOP Pattern in Primary Angle Closure and Primary Angle Closure Glaucoma Patients, Before and After LPI

A Prospective, Open Label Study Assessing the 24-hour Intraocular Pressure Pattern Monitored by SENSIMED Triggerfish® in Primary Angle Closure and Primary Angle Closure Glaucoma Patients, Before and After Laser Peripheral Iridotomy

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Sensimed AG · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to determine the relationship of the intraocular pressure patterns recorded during 2 sessions using Triggerfish, before and after elective laser peripheral iridotomy in angle closure glaucoma patients

Conditions

Interventions

TypeNameDescription
DEVICESENSIMED Triggerfish®SENSIMED Triggerfish® (TF) is a CE-marked portable device that monitors the 24-hour intraocular pressure (IOP) pattern by a wireless contact lens sensor (CLS) placed on the eye that sends its signals wirelessly via a periorbital patched adhesive antenna to a recorder. Upon completion, the recording can be transmitted to a computer for read-out and visualization

Timeline

Start date
2014-01-01
Primary completion
2014-03-01
Completion
2014-03-01
First posted
2013-07-23
Last updated
2014-05-13

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01906151. Inclusion in this directory is not an endorsement.

IOP Pattern in Primary Angle Closure and Primary Angle Closure Glaucoma Patients, Before and After LPI (NCT01906151) · Clinical Trials Directory