Laser showdown: where to zap the iris for better glaucoma control?
NCT ID NCT07195370
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests two different spots (temporal vs inferior) for a YAG laser iridotomy in people with angle-closure glaucoma. Each patient gets one spot in each eye, and doctors track pressure, symptoms, and complications over six months. The goal is to find which location is safer and more effective at lowering eye pressure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- YAG laser peripheral iridotomy (a procedure using a laser to create a small hole in the iris to improve fluid drainage)
- What this could lead to
- If successful, this could identify the best location for the laser procedure, potentially reducing complications and improving pressure control in glaucoma patients.
- What could go wrong
- This is a small, early-stage study with only 150 participants, and results may not apply to all patients. The procedure itself carries risks like bleeding or infection.
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
-
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 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2025
- Expected to finish
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Jan 2026
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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24 years and older
- 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:Diagnosis of Primary Angle-Closure Glaucoma. Adults (typically over 40 years old). Ability to provide informed consent. Narrow or closed anterior chamber angle (based on gonioscopy). Intraocular pressure (IOP) controlled with medication but requiring surgery. No previous iridotomy. Exclusion Criteria:econdary glaucoma. Active eye diseases (e.g., infection or inflammation). Advanced cataracts or lens-related issues. Severe visual impairment (e.g., less than 20/200 vision). Uncontrolled systemic diseases (e.g., diabetes or cardiovascular disease). Pregnancy or breastfeeding. Previous eye surgery (except for minor procedures). Inability to follow-up with scheduled visits. \-
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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.
Contacts and locations
Locations
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Isfahan University of Medical Sciences
Isfahan, Isfahan, 0098, Iran
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Other studies related to the condition(s) this trial covers.
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