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NCT07390890Recruiting

DSLT for Reducing Medication in Glaucoma

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

Source: ClinicalTrials.gov · Last updated 20 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
29 Jan 2026
Start date
10 Feb 2026
Primary completion date
26 Jan 2027
Lead sponsor
The Eye Institute of West Florida
NCT number
NCT07390890

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 10 Feb 2026 to the primary completion date, 26 Jan 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous glaucoma surgeries/interventions:
    • Patients who have undergone prior glaucoma-related procedures (e.g., trabeculectomy, laser trabeculoplasty, MIGS, or tube shunt).
  • Patients who have undergone cataract surgery within the prior 2 years.

Other illness

  • Secondary glaucoma:
    • Patients with secondary forms of glaucoma, such as angle-closure glaucoma, neovascular glaucoma, or glaucoma resulting from trauma or other systemic diseases.

Age

  • Other significant ocular conditions including advanced cataracts, retinal diseases (e.g., age-related macular degeneration), or any condition that might complicate the assessment of intraocular pressure (IOP) or visual function as deemed by the investigator.

Who the study is looking for

  • 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 IOP ≤21 mmHg.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Eye Institute of West Florida
Coordinator of this site? Confirm its status
LargoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.