AI outshines doctors in predicting cataract surgery success?
NCT ID NCT07713069
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This trial tests whether an artificial intelligence model called OCT-PRO can predict how well a person will see after cataract surgery more accurately than standard doctor predictions. The AI analyzes eye scans and other clinical data to forecast visual recovery. About 534 adults scheduled for cataract surgery will be randomly assigned to receive either an AI-assisted prediction or routine counseling. The goal is to see if the AI reduces the gap between expected and actual vision outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- OCT-PRO prediction model (a device that uses AI to analyze OCT images and clinical data)
- What this could lead to
- If successful, this AI tool could help doctors and patients set more realistic expectations for vision after cataract surgery, reducing disappointment.
- What could go wrong
- The AI may not outperform experienced clinicians in all cases, and its accuracy depends on high-quality eye scans. The trial is relatively small and early-stage.
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 534 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 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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18 to 90 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: * Age ≥18 years scheduled to undergo phacoemulsification with intraocular lens (Phaco+IOL) implantation. * Outpatient diagnosis of senile, complicated, or metabolic cataract. * For bilateral cataracts, the eye with more advanced disease will be included. Exclusion Criteria: * History of amblyopia or neuro-ophthalmic disease in the operative eye. * Poor-quality OCT images precluding clear visualization of fundus structures. * Previous intraocular surgery in the operative eye. * Hearing or intellectual impairment preventing adequate cooperation.
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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Other studies related to the condition(s) this trial covers.
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