Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04699864

Evaluation of NeoRetina Artificial Intelligence Algorithm for the Screening of Diabetic Retinopathy at the CHUM

Led by Centre hospitalier de l'Université de Montréal (CHUM) · Updated on 2024-09-19

630

Participants Needed

1

Research Sites

129 weeks

Total Duration

On this page

Sponsors

C

Centre hospitalier de l'Université de Montréal (CHUM)

Lead Sponsor

D

DIAGNOS Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This prospective study aims to validate if NeoRetina, an artificial intelligence algorithm developped by DIAGNOS Inc. and trained to automatically detect the presence of diabetic retinopathy (DR) by the analysis of macula centered eye fundus photographies, can detect this disease and grade its severity.

CONDITIONS

Official Title

Evaluation of NeoRetina Artificial Intelligence Algorithm for the Screening of Diabetic Retinopathy at the CHUM

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years old and older
  • Ability to provide informed consent
  • Diagnosis of diabetes: type 1 diabetes for at least 5 years or type 2 diabetes
  • Diabetic patient followed or referred by a CHUM physician, including endocrinologist follow-up, hospitalization at CHUM, or on the Ophthalmology Clinic waiting list for DR evaluation
Not Eligible

You will not qualify if you...

  • Patients younger than 18 years old
  • Inability to provide informed consent
  • Previous treatment (surgery, laser, injection, etc.) for any retinal condition such as age-related macular degeneration or retinal vascular occlusion

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre hospitalier de l'Université de Montréal

Montreal, Quebec, Canada, H2X 0A9

Actively Recruiting

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Research Team

M

Marie-Catherine Tessier, MSc

CONTACT

K

Karim Hammamji, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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