Laser procedure could offer new hope for pseudoexfoliation glaucoma patients
NCT ID NCT07401290
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a non-invasive laser procedure called direct selective laser trabeculoplasty (DSLT) in 40 adults with pseudoexfoliation glaucoma. The goal is to see if the laser can safely lower eye pressure by at least 20% at 6 and 12 months. Participants will have their eye pressure measured after stopping any glaucoma medications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Direct selective laser trabeculoplasty (DSLT) - a non-invasive laser procedure to improve fluid drainage in the eye
- What this could lead to
- If successful, this laser treatment could offer a safe, non-drug option to control eye pressure in people with pseudoexfoliation glaucoma.
- What could go wrong
- This is a small, early-stage study with only 40 participants and no comparison group. The results may not apply to all patients, and the procedure may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients diagnosed with pseudoexfoliation glaucoma (PXFG), with optic neuropathy consistent with glaucomatous damage of any severity * Open iridocorneal angle by gonioscopy, defined as a Shafer Grade II or greater * Treatment naive, or washed out IOP ranging from ≥18-35 mmHg * Able to complete medication washout safely and all follow-up visits * Participants must have a best correct visual acuity of 20/40 or better in the study eye(s), be able to undertake a reliable Humphrey visual field (HVF) (defined as fixation losses, false positives and false negatives less than 33%), and must have field loss no worse than -20 dB in treatment eye Exclusion Criteria: * Any contraindication to SLT or unable to have DSLT * Angle closure glaucoma or any other types of glaucoma other than PXFG * Prior incisional glaucoma surgery or glaucoma-related procedures in the study eye * Any prior refractive surgery * H/o LPI within last 6 months * A history of any significant cataract required during study duration or cataract surgery in the last 6 months * Prior laser trabeculoplasty (ALT/SLT) * History of ocular inflammation and infection * Patients who are pregnant or have any clinically relevant systemic disease that may prevent them from reliably completing follow-up visits * Vulnerable populations that cannot provide proper informed consent will not be enrolled, such as children, prisoners, handicapped, or mentally disabled persons, or economically or educationally disadvantaged persons
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Vance Thompson Vision
Alexandria, Minnesota, 56308, United States
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Vance Thompson Vision
Omaha, Nebraska, 68137, United States
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Vance Thompson Vision
Fargo, North Dakota, 58078, United States
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