VeriSee AI for screening macular degeneration and diabetic retinopathy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial will use the VeriSee AI system to analyze color fundus photographs and produce rapid detection results for ophthalmologists to use as diagnostic support. Participants will have fundus images taken in non-retinal ophthalmology clinics and their clinical history recorded for comparison with standard clinical diagnosis. The study will compare the AI-assisted readings to ophthalmologist decisions and measure clinical and cost-effectiveness outcomes. The goal is to determine whether integrating VeriSee improves screening efficiency, diagnostic consistency, and access to care.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* VeriSee AMD is used in non-retinal subspecialty ophthalmology clinics for adults aged 50 and above.
* VeriSee DR is used in non-retinal subspecialty clinics for diabetic patients aged 20 and above.

Exclusion Criteria:

* The patient does not agree to participate in the trial or is unable to provide informed consent.

Where it's running

• National Taiwan University Hospital
  Taipei, Taiwan, Taiwan Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.