Pivotal Trial of an Automated AI-based System for Early Diagnosis and Prediction of Late Age-related Macular Degeneration
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| iHealthScreen Inc. | Richmond Hill | New York | Recruiting |
More iHealthScreen Inc trials in the USA
Other trials for the same condition
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