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Clinical Trials/NCT00485108
NCT00485108
Completed
Not Applicable

Anti-inflammatory Therapy Following Selective Laser Trabeculoplasty (SLT): A Randomized, Masked, Placebo Controlled Study

Queen's University1 site in 1 country120 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
prednisolone 1%
Conditions
Primary Open Angle Glaucoma
Sponsor
Queen's University
Enrollment
120
Locations
1
Primary Endpoint
Intraocular pressure lowering effect
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The type of anti-inflammatory medication used post selective laser trabeculoplasty (SLT) may have an impact on the intra-ocular pressure (IOP) lowering effect of SLT. This study will evaluate the IOP lowering effect of SLT following the topical administration of one of the following: prednisolone 1%, ketorolac 0.5% or artificial tears.

Detailed Description

Patients who have been chosen to undergo SLT for glaucoma will be randomized to receive one of prednisolone 1%, ketorolac 0.5% or artificial tears four times a day for 5 days following administration of the laser treatment. The IOP will be measured at various time points following SLT: 1 hour, 2 days, 1 week, 1 month, 3 months, 6 months, and 1 year.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
December 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Robert Campbell

Assistant Professor

Queen's University

Eligibility Criteria

Inclusion Criteria

  • primary open angle glaucoma, pseudo exfoliation glaucoma

Exclusion Criteria

  • previous incisional glaucoma surgery

Arms & Interventions

1

Prednisolone 1% eye drop

Intervention: prednisolone 1%

2

ketorolac 0.5% eye drop

Intervention: ketorolac 0.5%

3

Artificial Tears (methyl cellulose eye drop)

Intervention: Artificial Tears (Methyl cellulose drops)

Outcomes

Primary Outcomes

Intraocular pressure lowering effect

Time Frame: 1 hour, 2 days, 1 month, 3 months, 6 months and 1 year

Secondary Outcomes

  • intraocular pressure elevation(1 hour, 2 days, 1 month)

Study Sites (1)

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