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NOT YET RECRUITING
NCT07465913
PHASE4

Rocklatan vs Latanoprost Post-DSLT

Sponsor: Eye Centers of Southeast Texas

View on ClinicalTrials.gov

Summary

This is a randomized, double-masked, single-site, prospective, contralateral eye study designed to evaluate the outcomes of Direct Selective Laser Trabeculoplasty (DSLT) followed by the addition of combination netarsudil and latanoprost (Rocklatan) versus latanoprost monotherapy. The study will be conducted at one investigational site. The primary endpoint is the change in mean diurnal intraocular pressure (IOP) from baseline (post DSLT and post washout) at visit 3 between the two groups. Secondary endpoints include the change in mean IOP from baseline at each timepoint (8am, 12pm, 4pm) at visit 3 between groups, and the mean percentage decrease in IOP from baseline for each group. Assessments will be conducted at three key visits: Visit 1 (Screening Phase and DSLT Procedure on Day 0), Visit 2 (Baseline Visit post washout at Week 8), and Visit 3 (Follow-Up Visit 1 at Week 12). Each visit will include specific examinations and measurements such as visual field and OCT imaging, diurnal IOP measurements, and documentation of adverse events.

Official title: Outcomes of Direct Selective Laser Trabeculoplasty With the Post-treatment Addition of Combination Netarsudil and Latanoprost vs Latonoprost Monotherapy

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

36

Start Date

2026-05-06

Completion Date

2027-05-06

Last Updated

2026-03-12

Healthy Volunteers

No

Conditions

Interventions

DRUG

Rocklatan 0.02%-0.005% Ophthalmic Solution

netarsudil and latanoprost 0.02%/0.005%

DRUG

Latanoprost 0.005% Ophthalmic Solution

Latanoprost 0.005%

Locations (1)

Eye Centers of Southeast Texas

Beaumont, Texas, United States