Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants receive the Voyager DSLT device treatment for glaucoma.
1 treatment visit (in-person)
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
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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