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Anti-inflammatory Therapy Following Selective Laser Trabeculoplasty

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00485108
Enrollment
120
Registered
2007-06-12
Start date
2007-01-31
Completion date
2014-12-31
Last updated
2015-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Open Angle Glaucoma, Pseudoexfoliation Glaucoma

Keywords

primary open angle glaucoma, pseudoexfoliation glaucoma, selective laser trabeculoplasty, intra ocular pressure, anti-inflammatory therapy, prednisolone acetate 1%, ketorolac tromethamine 0.5%

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.

Interventions

eye drop once in each eye treated, 4 times / day for 5 days post-laser

eye drop once in each eye treated, 4 times / day for 5 days post-laser

DRUGArtificial Tears (Methyl cellulose drops)

eye drop once in each eye treated, 4 times / day for 5 days post-laser

Sponsors

Pfizer
CollaboratorINDUSTRY
Glaucoma Research Society of Canada
CollaboratorOTHER
Queen's University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* primary open angle glaucoma, pseudo exfoliation glaucoma

Exclusion criteria

* previous incisional glaucoma surgery

Design outcomes

Primary

MeasureTime frame
Intraocular pressure lowering effect1 hour, 2 days, 1 month, 3 months, 6 months and 1 year

Secondary

MeasureTime frame
intraocular pressure elevation1 hour, 2 days, 1 month

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026