Evaluation of NeoRetina Artificial Intelligence Algorithm for the Screening of Diabetic Retinopathy at the CHUM (DR-NeoRetina)

The Use of Artificial Intelligence in the Early Detection and the Follow-Up of Diabetic Retinopathy of Diabetic Patients Followed at the CHUM: Evaluation of NeoRetina Automated Algorithm (DIAGNOS Inc.)

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.

Study Overview

Detailed Description

More than 880 000 Quebecers (more than 10% of the population) suffer from diabetes, which is the main cause of blindness in diabetic adults under 65 years of age, and around 40% of people with diabetes suffer from diabetic retinopathy (DR). The early detection of DR and a regular follow-up is thus crucial to prevent the progression of this disease.

However, the public health care system in Quebec does not actually have the capacity to allow all people with diabetes to see an ophthalmologist within a short delay. Artificial intelligence might help in screening DR and in refering to eye doctors only patients who suffer from this eye disease.

The investigators of this study hypothesize that artificial intelligence (AI) is a useful technology for the screening of diabetic retinopathy (DR) that can detect the absence or the presence of DR with an efficiency and an accuracy similar to that of an ophthalmological evaluation.

The goal of this study is to compare the screening results of DR obtained with NeoRetina pure artificial intelligence algorithm (automated analysis of color photos of the retina) with the results of a routine ophthalmological evaluation done in a clinical context at the Centre hospitalier de l'Université de Montréal (CHUM).

The main objective of this study is to determine if artificial intelligence (AI) could be a useful technology for the early detection and the follow-up of diabetic retinopathy (DR).

The first specific objective is to determine the efficiency and the accuracy of NeoRetina (DIAGNOS Inc.) automated algorithm for the screening and the grading of the severity of diabetic retinopathy (DR) by the analysis of eye fundus images from diabetic patients compared to that of an eye examination done by an ophthalmologist in a clinical context.

The second specific objective is to evaluate if NeoRetina can determine, with efficiency and accuracy, the absence of diabetic retinopathy (DR), the presence of diabetic retinopathy (DR) and the severity of the disease.

Recruited diabetic participants will be screened for DR by AI with NeoRetina. Participants will also have a full eye examination (blind assessment) with an ophthalmologist of the CHUM in order to determine if they suffer from this eye complication of diabetes.

The results of the screening done by AI with NeoRetina will be compared to those of the ocular evaluation done by an ophthalmologist. Ophthalmologists from the CHUM will also revise the retinal images acquired by DIAGNOS (blind assessment) in order to determine if DR is present and will manually grade the severity of the disease.

Study Type

Interventional

Enrollment (Estimated)

630

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Patients of 18 years old and older;
  2. Ability to provide informed consent;
  3. Diagnostic for diabetes : 3a) Type 1 diabetes of a lest 5 years of evolution; or 3b) Type 2 diabetes;
  4. Diabetic patient followed and refered by a physician of the Centre hospitalier de l'Université de Montréal (CHUM) : 4a) followed by an endocrinologist of the CHUM; or 4b) hospitalized at the CHUM; or 4c) on the waiting list of the Ophthalmology Clinic of the CHUM for the evaluation of DR.

Exclusion Criteria:

  1. Patients less than 18 years old;
  2. Inability to provide informed consent;
  3. Patient who already had a treatment (surgery, laser, injection, etc.) for any retinal condition : Age-related macular degeneration (AMD), retinal vascular occlusion (RVO); etc.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Diabetic Retinopathy (DR)
Screening of DR with artificial intelligence (NeoRetina algorithm) and diagnostic evaluation with a standard of care ophthalmological examination.
Macula-centered eye color fundus photos will be acquired by DIAGNOS team using a non-mydriatic digital camera (without pupil dilation). After a numerical treatment, retinal images will be analyzed by NeoRetina artificial intelligence (AI) algorithm in order to find eye lesions characteristics of diabetic retinopathy (DR) and diabetic macular edema (DME). The severity of DR and DME will be graded by NeoRetina according to the ''Early Treatment Diabetic Retinopathy Study'' (ETDRS) international classification standards.
Standard of care eye examination (blind assessment) will be performed by an ophthalmologist of the CHUM in order to find lesions characteristics of diabetic retinopathy (DR) and diabetic macular edema (DME). The severity of DR and DME will be graded by the doctor according to the ''Early Treatment Diabetic Retinopathy Study'' (ETDRS) international classification standards.
Ophthalmologists of the CHUM will revise the macula-centered eye color photos acquired by DIAGNOS in order to find lesions characteristics of diabetic retinopathy (DR) and diabetic macular edema (DME). The severity of DR and DME will be graded (blind assessment) according to the ''Early Treatment Diabetic Retinopathy Study'' (ETDRS) international classification standards.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Artificial Intelligence - Absence or Presence of Diabetic Retinopathy (DR)
Time Frame: Baseline

Analysis of retinal images by artificial intelligence (NeoRetina) to determine the absence or the presence of diabetic retinopathy (DR)

  • R0 : No DR
  • R+ : Presence of DR
Baseline
Eye Examination - Absence or Presence of Diabetic Retinopathy (DR)
Time Frame: Baseline

Eye examination done by an ophthalmologist to determine the absence or the presence of diabetic retinopathy (DR) (blind assessment)

  • R0 : No DR
  • R+ : Presence of DR
Baseline
Manual Analysis of Retinal Images - Absence or Presence of Diabetic Retinopathy (DR)
Time Frame: Baseline

Manual analysis of retinal images acquired by Diagnos by an ophthalmologist of the CHUM to determine the absence or the presence of diabetic retinopathy (DR) (blind assessment)

  • R0 : No DR
  • R+ : Presence of DR
Baseline
Artificial Intelligence - Severity of Diabetic Retinopathy (DR)
Time Frame: Baseline

Analysis of retinal images by artificial intelligence (NeoRetina) to grade the severity of diabetic retinopathy (DR)

  • R1 - Mild NPDR: Mild Nonproliferative Diabetic Retinopathy
  • R2 - Moderate NPDR: Moderate Nonproliferative Diabetic Retinopathy
  • R3 - Severe NPDR : Severe Nonproliferative Diabetic Retinopathy
  • R4 - PDR : Proliferative Diabetic Retinopathy
Baseline
Eye Examination - Severity of Diabetic Retinopathy (DR)
Time Frame: Baseline

Eye examination done by an ophthalmologist to grade the severity of diabetic retinopathy (DR) (blind assessment)

  • R1 - Mild NPDR: Mild Nonproliferative Diabetic Retinopathy
  • R2 - Moderate NPDR: Moderate Nonproliferative Diabetic Retinopathy
  • R3 - Severe NPDR : Severe Nonproliferative Diabetic Retinopathy
  • R4 - PDR : Proliferative Diabetic Retinopathy
Baseline
Manual Analysis of Retinal Images - Severity of Diabetic Retinopathy (DR)
Time Frame: Baseline

Manual revision of retinal images acquired by Diagnos by an ophthalmologist of the CHUM to grade the severity of diabetic retinopathy (DR) (blind assessment)

  • R1 - Mild NPDR: Mild Nonproliferative Diabetic Retinopathy
  • R2 - Moderate NPDR: Moderate Nonproliferative Diabetic Retinopathy
  • R3 - Severe NPDR : Severe Nonproliferative Diabetic Retinopathy
  • R4 - PDR : Proliferative Diabetic Retinopathy
Baseline
Artificial Intelligence - Absence or Presence of Diabetic Macular Edema (DME)
Time Frame: Baseline

Analysis of retinal images by artificial intelligence (NeoRetina) to determine the absence or the presence of diabetic macular edema (DME)

  • M0 : No DME
  • M+ : Presence of DME
Baseline
Eye Examination - Absence or Presence of Diabetic Macular Edema (DME)
Time Frame: Baseline

Eye examination done by an ophthalmologist to determine the absence or the presence of diabetic macular edema (DME) (blind assessment)

  • M0 : No DME
  • M+ : Presence of DME
Baseline
Manual Analysis of Retinal Images - Absence or Presence of Diabetic Macular Edema (DME)
Time Frame: Baseline

Manual analysis of retinal images acquired by Diagnos by an ophthalmologist of the CHUM to determine the absence or the presence of diabetic macular edema (DME) (blind assessment)

  • M0 : No DME
  • M+ : Presence of DME
Baseline
Artificial Intelligence - Severity of Diabetic Macular Edema (DME)
Time Frame: Baseline

Analysis of retinal images by artificial intelligence (NeoRetina) to grade the severity of diabetic macular edema (DME)

  • M1 : Non Central DME
  • M2 : Central DME
Baseline
Eye Examination - Severity of Diabetic Macular Edema (DME)
Time Frame: Baseline

Eye examination done by an ophthalmologist to grade the severity of diabetic macular edema (DME) (blind assessment)

  • M1 : Non Central DME
  • M2 : Central DME
Baseline
Manual Analysis of Retinal Images - Severity of Diabetic Macular Edema (DME)
Time Frame: Baseline

Manual analysis of retinal images acquired by Diagnos by an ophthalmologist of the CHUM to grade the severity of diabetic macular edema (DME) (blind assessment)

  • M1 : Non Central DME
  • M2 : Central DME
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Performance of NeoRetina Algorithm - Diabetic Retinopathy (DR)
Time Frame: 3 years

The performance of NeoRetina algorithm for the detection and the grading of diabetic retinopathy (DR) will be evaluated.

The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) and area under the receiver operating characteristic curve (AUC, 95% CI) will be calculated.

The levels of agreement will be determined by kappa analyses.

3 years
Performance of NeoRetina Algorithm - Diabetic Macular Edema (DME)
Time Frame: 3 years

The performance of NeoRetina algorithm for the detection and the grading of diabetic macular edema (DME) will be evaluated.

The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) and area under the receiver operating characteristic curve (AUC, 95% CI) will be calculated.

The levels of agreement will be determined by kappa analyses.

3 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Karim Hammamji, MD, Centre hospitalier de l'Université de Montréal (CHUM)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 10, 2024

Primary Completion (Estimated)

April 1, 2025

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

December 16, 2020

First Submitted That Met QC Criteria

January 5, 2021

First Posted (Actual)

January 7, 2021

Study Record Updates

Last Update Posted (Actual)

September 19, 2024

Last Update Submitted That Met QC Criteria

September 16, 2024

Last Verified

September 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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