Clinical Trials Directory

Trials / Completed

CompletedNCT01906138

An Open Label Study Assessing the 24-hour Intraocular Pressure Pattern in PAC and PACG Patients, Before and After Laser Peripheral Iridotomy

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
Completed
Phase
N/A
Study type
Interventional
Enrollment
27 (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®All eligible patients will be assigned to 24-hour intraocular pressure recording using Triggerfish

Timeline

Start date
2013-07-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2013-07-23
Last updated
2014-08-26

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT01906138. Inclusion in this directory is not an endorsement.

An Open Label Study Assessing the 24-hour Intraocular Pressure Pattern in PAC and PACG Patients, Before and After Laser (NCT01906138) · Clinical Trials Directory