One drop before the laser: could this simple step save your sight?
NCT ID NCT07729189
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
This trial tests whether a single drop of timolol maleate, given just before Nd:YAG laser capsulotomy, can prevent a short-term rise in eye pressure. The study includes adults who developed clouding of the lens capsule months after cataract surgery. Half receive the timolol drop; the other half receive standard care. Eye pressure is measured before and one hour after the laser to see if the drop makes a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a single drop of 0.5% timolol maleate eye solution given just before laser surgery
- What this could lead to
- If it works, a single drop before laser treatment could become a simple, low-cost way to protect eyes from pressure spikes.
- What could go wrong
- This is a small, early-stage trial. The benefit may be small or not apply to all patients. Timolol can cause side effects like eye irritation or slowed heart rate.
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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210 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Sep 2025
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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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18 to 65 years
- 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: * Adults aged 18-65 years * Male or female participants * Diagnosed with posterior capsule opacification after cataract surgery * Posterior capsule opacification present for at least 3 months * Scheduled to undergo Nd:YAG laser posterior capsulotomy Exclusion Criteria: * History or documented diagnosis of glaucoma * Baseline intraocular pressure greater than 21 mmHg before the procedure
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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
-
CMH Institute of Medical Sciences
Multan, Punjab Province, 66000, Pakistan
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Other studies related to the condition(s) this trial covers.
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