Actively Recruiting

All Genders
NCT07390890

DSLT for Reducing Medication in Glaucoma

Led by The Eye Institute of West Florida · Updated on 2026-04-20

60

Participants Needed

1

Research Sites

50 weeks

Total Duration

On this page

Sponsors

T

The Eye Institute of West Florida

Lead Sponsor

S

Sengi

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

DSLT for Reducing Medication in Glaucoma

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients scheduled to undergo DSLT treatment in one or both eyes
  • Diagnosis of ocular hypertension or primary open angle glaucoma
  • Medically controlled on 1-3 topical ocular hypotensive agents with IOP 6421 mmHg
Not Eligible

You will not qualify if you...

  • Prior glaucoma surgeries or interventions such as trabeculectomy, laser trabeculoplasty, MIGS, or tube shunt
  • Cataract surgery within the prior 2 years
  • Secondary forms of glaucoma including angle-closure, neovascular, or glaucoma from trauma or systemic diseases
  • Other significant eye conditions like advanced cataracts or retinal diseases that could affect IOP or visual function assessment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Eye Institute of West Florida

Largo, Florida, United States, 33770

Actively Recruiting

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Research Team

R

Renee Bondurant

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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