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Study identifier: NCT04416724 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Phacoemulsification vs SLT as Initial Treatment for Pseudoexfoliation Glaucoma

Condition: Pseudoexfoliation Glaucoma  ·  Sponsor: Nova Scotia Health Authority

PhaseNA
Planned participants200
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

The Canadian Pseudoexfoliation Glaucoma Study 1 is a randomized clinical trial that aims to compare two initial treatment options - Selective Laser Trabeculoplasty (SLT) and Phacoemulsification (PHACO) - in newly diagnosed patients with pseudoexfoliation and need to lower the intraocular pressure. Patients with pseudoexfoliation and a recent decision to lower the intraocular pressure, who also have early asymptomatic lens opacification will be recruited and randomized to receive either SLT or PHACO. Patients will be followed for 2 years according to a target IOP protocol based on the Canadian Ophthalmological Society Glaucoma guidelines. Patients who do not achieve the target IOP with the initial randomization procedure will receive IOP lowering medications. The main outcome of interest will be the proportion of subjects who need IOP lowering medications after 2 years. Secondary outcomes include IOP reduction, time to need medications, patient reported outcomes in terms of visual function, and occurrence of adverse effects. To obtain longer follow-up information beyond two years, a chart review will be done 5 and 10 years after randomization.

This description comes directly from the study's public registry record.

Talk to the study team

Marcelo Nicolela, MD  ·  902-473-2839  ·  nicolela@dal.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Nova Scotia HealthHalifax, Nova Scotia, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT04416724