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
| Type | Name | Description |
|---|---|---|
| DRUG | brimonidine 0.1% | 1 drop, 1 hour prior to selective laser trabeculoplasty (SLT) |
| DRUG | Apraclonidine 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.