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AI Co-Pilot aims to sharpen eye disease diagnoses

NCT ID NCT07401459

Knowledge-focused Sponsor: The Hong Kong Polytechnic University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests an AI tool called EyeAgent that helps eye doctors make decisions. About 300 people visiting eye clinics in Hong Kong and mainland China will take part. The AI reviews patient images and history to suggest diagnoses and treatments. The goal is to see if using the AI improves accuracy, efficiency, and doctor satisfaction compared to standard care.

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

About 300 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

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

6 to 75 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: 1. Outpatient participants aged 6 to 75 years. 2. Participants who undergo ophthalmic examinations for medical purposes during the study period. 3. Participants who can produce clear ophthalmic images in both eyes. 4. Agree to participate in this study with written informed consent: 1. Participants aged 18 years or older provide their own consent. 2. Participants aged 6-17 years require consent from a parent or legal guardian. Exclusion Criteria: 1. Participants who are reluctant to participate in this study. 2. Participants presenting with acute or emergency ocular conditions requiring immediate intervention. 3. Participants with poor quality of ophthalmic images, including blurriness, artifacts, underexposure, or overexposure. 4. Other unsuitable reasons determined by the evaluators.

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Conditions

The condition(s) this trial relates to.

eye disorder retinal disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Ai agent Eye disease Large language models Ophthalmology Retinal disease

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • The Hong Kong Polytechnic University

    Hong Kong, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.