Clinical Trial

DSLT for Reducing Medication in Glaucoma

Recruiting
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Summary
This is a prospective, single arm, open label study conducted at a single site to evaluate the efficacy of Direct Selective Laser Trabeculoplasty (DSLT) in reducing medication burden in patients with medically controlled ocular hypertension or primary open angle glaucoma. The study will assess the primary endpoint of reduction in medication count at 6 months compared to baseline. Secondary endpoints include IOP reduction compared to baseline (both percentage and absolute), complete success rate (no increase in IOP without medications), proportion of eyes needing medication at 6 months, and any secondary surgical interventions at 6 months post-DSLT. Participants will undergo DSLT with 120 shots, 400 µm spot size, and 1.8mJ fixed energy delivered at the limbus over 2.4 seconds. Follow-up visits will occur at 1 month, 3 months, and 6 months post-procedure, with IOP measured using a calibrated Goldmann tonometer.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-29.
Trial Details
NCT Number NCT07390890
Lead Sponsor The Eye Institute of West Florida
Collaborators: Sengi
Conditions Primary Open Angle Glaucoma, Ocular Hypertension
Enrollment 60 participants
Start Date 2026-02-10
Primary Completion 2027-01-26 (estimated)
Study Completion 2027-01-26 (estimated)
Updated on ClinicalTrials.gov 2026-04-20