Clinical Trials Directory

Trials / Unknown

UnknownNCT00567411

Comparison of the Alpha-2 Agonists for Prevention of Intraocular Pressure Elevation After Selective Laser Trabeculoplasty

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
43 (estimated)
Sponsor
Walter Reed Army Medical Center · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to compare the safety and efficacy of two drops used to lower eye pressure when given prior to a glaucoma laser procedure.

Detailed description

This is a prospective randomized double blind trial of patients undergoing selective laser trabeculoplasty for primary open angle glaucoma and ocular hypertension. Enrolled patients are randomized to receive one drop of brimonidine 0.1% in one eye and one drop of apraclonidine 0.5% in the fellow eye. The trabecular meshwork in both eyes of each enrolled patient is treated 360 degrees at the same sitting. Intraocular pressure is measured in each eye one hour before applying the study medications and at one hour and one week after laser surgery.

Conditions

Interventions

TypeNameDescription
DRUGbrimonidine 0.1%1 drop, 1 hour prior to selective laser trabeculoplasty (SLT)
DRUGApraclonidine 0.5%1 drop applied 1 hour prior to SLT

Timeline

Start date
2006-08-01
Completion
2009-06-01
First posted
2007-12-05
Last updated
2007-12-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00567411. Inclusion in this directory is not an endorsement.