Ireland
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Recruiting Observational

Pivotal Trial of an Automated AI-based System for Early Diagnosis and Prediction of Late Age-related Macular Degeneration

NCT07084883 · tracked via the Priya Life Science USA tracker
Sponsor
iHealthScreen Inc
Phase
Observational
Started
2024-08-01
Last updated
2025-08-28

Condition(s) studied

Age-related Macular Degeneration (AMD)

Investigational drug(s) / intervention(s)

No intervention.

No intervention.: No intervention. Evaluate the automated AMD screening software.

Study summary

The purpose of this study is to perform a pivotal trial of iPredict, an automated AI-based system for early diagnosis and prediction of late AMD in primary care and ophthalmology settings. Patients will be invited to participate in this study by having non-dilated photos of their eyes taken by an FDA approved fundus camera (DRSPlus from Centervue Inc., CA), at their primary care doctor's office or general ophthalmologist office. The photos will then be transmitted securely and analyzed by computer in the cloud (telemedicine features). Sufficient accuracy of the automatic system has been established compared to the ophthalmologist's diagnosis. In this study, we aim to validate the system against the prospectively taken OCT image and color fundus images.

Eligibility

Sex
ALL
Min age
50 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Subjects will be recruited if willing and able to comply with clinic visit and study-related procedures, and provide signed informed consent Exclusion Criteria: * Already diagnosed with AMD, unable to provide informed consent and currently under treatment of retinal disease.

Primary outcome measure(s)

  • Referable and non-referable AMD. And Predict the Incidence of AMD in 1 year or 2-year. — 1 year or 2-year
    Referable and non-referable AMD. And Predict the Incidence of AMD in 1 year or 2-year.

Trial sites (1)

FacilityCityRegionStatus
iHealthScreen Inc. Richmond Hill New York Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07084883 on ClinicalTrials.gov ↗ ← All trials in the USA