Actively Recruiting

All Genders
ID07390890

Efficacy of Direct Selective Laser Trabeculoplasty (DSLT) for Reducing Medication Burden in Medically Controlled Patients With Ocular Hypertension or Primary Open Angle Glaucoma

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

60

Participants Needed

1

Research Sites

N/A

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

Researchers are evaluating Direct Selective Laser Trabeculoplasty (DSLT) to see if it can reduce the number of medications needed for patients with medically controlled ocular hypertension or primary open angle glaucoma. This prospective, open-label study will measure how well DSLT lowers medication use and intraocular pressure (IOP), as well as monitor the need for additional medications or surgeries over six months. The study is sponsored by The Eye Institute of West Florida and focuses on maintaining target IOP with fewer medications. Participants will receive DSLT treatment using the Voyager DSLT device, which delivers 120 laser shots at the eye's limbus over 2.4 seconds. The laser settings include a 400 micrometer spot size and fixed energy of 1.8 mJ. The procedure aims to reduce medication burden while monitoring IOP. Follow-up visits are scheduled at 1, 3, and 6 months after treatment to assess outcomes. During the study, participants will have their IOP measured at each follow-up using a calibrated Goldmann tonometer. Researchers will track changes in medication use, IOP levels, and the need for any secondary surgical interventions. The primary outcome is the reduction in glaucoma medications at six months compared to baseline. Secondary measures include IOP changes, success rates without medication increase, and medication use proportions. Total study participation lasts six months post-treatment.

CONDITIONS

Brief 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 (POAG)
  • Medically controlled on 1-3 topical ocular hypotensive agents with intraocular pressure (IOP) �3C= 21 mmHg
Not Eligible

You will not qualify if you...

  • Previous 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 trauma-related glaucoma
  • Significant ocular conditions like advanced cataracts or retinal diseases that complicate IOP or visual function assessment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - 1 day

Participants receive the Voyager DSLT device treatment for glaucoma.

1 treatment visit (in-person)

Post-operative Follow-up

Duration - 6 months

Participants are followed after the DSLT treatment to monitor intraocular pressure and medication requirements.

Multiple follow-up visits over 6 months

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

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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