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OphtAI Diagnostic Performance Validation for Automated Screening of Eye Diseases

Validation of OphtAI Software Diagnostic Performance for Automated Screening of Diabetic Retinopathy, Diabetic Macular Edema, Glaucoma, ARM and ARMD: a Multicentre Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05752045
Acronym
OPHTAI-EVAL
Enrollment
1389
Registered
2023-03-02
Start date
2023-06-28
Completion date
2024-03-31
Last updated
2023-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Age-Related Macular Degeneration, Age-related Maculopathy, Diabetic Macular Edema, Diabetic Retinopathy, Glaucoma

Keywords

OphtAI, Artificial intelligence, Computer-aided diagnosis, Automated screening, Medical Device, Diabetic patient, Diabetic Retinopathy, Diabetic Macular Edema, Age-Related Macular Degeneration, Age-related Maculopathy, Glaucoma, Evolucare OphtAI

Brief summary

Evolucare OphtAI is a medical device offering automated, artificial intelligence powered, screening capabilities for Diabetic Retinopathy, Diabetic Macular Edema, Glaucoma, ARM and AMD, whose performances will by tested through the OphtAI-EVAL.

Detailed description

OphtAI-Eval: is a prospective, multicentre, post-marketing clinical follow-up study (SCAC) of diagnostic validation (comparative vs gold standard). It aims to: validate the diagnostic performance of the OphtAI software for the automated screening of diabetic retinopathy, diabetic macular edema, glaucoma, ARM and AMD. Evolucare OphtAI is a medical imaging console for ophthalmology, interfaced with Evolucare Imaging. It allows the detection, by statistical learning algorithms, of the following ocular pathologies using photographs of the retina: * Diabetic retinopathy (DR) (including gradation), * Diabetic macular edema (DME) * Age-related macular degeneration (AMD) * Age-related maculopathy (ARM, early form of AMD), * Glaucoma. Evolucare OphtAI, is available on the French market since March 2019.

Interventions

DEVICEEye Fundus Double Capture for Eye Diseases Screening with OphtAI Medical Device

Double ophthalmological imaging capture of eye fundus with different fundus camera to screen patient for various eye diseases.

Sponsors

Slb Pharma
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
CollaboratorOTHER
BPIfrance
CollaboratorOTHER
Evolucare Technologies
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Masking description

Ground truth and Results being obtained in the end of recruitment and imaging collection, there are no effects on participant or care provider. Also, experts won't be aware of AI results and vice versa.

Intervention model description

Imaging and clinical data will be collected from patients to be reviewed by an expert reader group providing ground truth, and the medical device will be tested against this ground truth

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Doesn't not accept healthy volunteers as diabetic patients are needed, still they may be free of any eye diseases. Inclusion Criteria: The characteristics required for a subject to take part in the research are * Male or female over 18, * Type 1 or 2 diabetic, * Presenting for screening for diabetic retinopathy, * Beneficiary of a social security scheme, * For whom written consent has been obtained for participation in the protocol.

Exclusion criteria

The following characteristics do not allow the subject to take part in the research: * Patient with known DR, more severe than minimal, including having been treated, * Any other condition that, in the opinion of the health professionals, may interfere with their ability to complete the study or may present a significant risk, * Presence of social, medical and/or psychological factors that may compromise the patient's adherence to the protocol, * Simultaneously participating in another clinical research protocol or having recently participated in another research study for which the exclusion period would not be completed. Patients who participate in this research will not be able to participate in another research at the same time. However, there is no exclusion period at the end of this research for participation in any other study.

Design outcomes

Primary

MeasureTime frameDescription
Referable Diabetic Retinopathy screening sensitivity/specificity1 yearReferable Diabetic Retinopathy screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for RDR-EOphtha and RDR-OphDiaT\_full algorithms

Secondary

MeasureTime frameDescription
Diabetic retinopathy grading + RDR-EOphtha algorithms combination sensitivity/specificity for RDR detection1 yearReferable Diabetic Retinopathy screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for RDR-EOphtha and RD grading algorithms combination
Diabetic retinopathy grading + RDR-OphDiaT_full algorithms combination sensitivity/specificity for RDR detection1 yearReferable Diabetic Retinopathy screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for RDR-OphDiaT\_full and RD grading algorithms combination
Diabetic retinopathy grading + RDR-EOphtha +DME algorithms combination sensitivity/specificity for RDR detection1 yearReferable Diabetic Retinopathy screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for RDR-EOphtha, RD grading and DME algorithms combination
Diabetic retinopathy grading + RDR-OphDiaT_full +DME algorithms combination sensitivity/specificity for RDR detection1 yearReferable Diabetic Retinopathy screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for RDR-OphDiaT\_full , RD grading and DME algorithms combination
Diabetic Macular Edema algorithm sensitivity/specificityfor DME detection1 yearDiabetic Macular Edema screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for DME algorithm
Diabetic retinopathy grading sensitivity/specificity1 yearDiabetic retinopathy grading performance (OphtAI software vs Expert reader) for each grading sub algorithms (sensitivity/specificity) and globally (accuracy/agreement ratio)
Age-Related Maculopathy algorithm (drusen) sensitivity/specificity for ARM detection1 yearARM screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for ARM algorithm, for all forms and for either macular or peripheric drusen, or for either hard/soft drusen
Glaucoma algorithms sensitivity/specificity for Glaucoma suspicion1 yearGlaucoma screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for Glaucoma algorithms
Quality algorithm accuracy for quality assessment1 yearBad quality images sensitivity/specificity evaluation (OphtAI software vs Expert reader) for quality assessment algorithms
Laterality determination algorithm accuracy for laterality assessment1 yearLaterality accuracy of OphtAI software vs Expert reader for laterality determination algorithm
Age-Related Macular Degeneration algorithm sensitivity/specificity for AMD detection1 yearAMD screening sensitivity/specificity evaluation (OphtAI software vs Expert reader) for AMD algorithm, for all forms and for either atrophic or neovascular AMD

Countries

France

Contacts

Primary ContactOphélie Flageul
o.flageul@slbpharma.com02 23 06 11 13
Backup ContactLaurent Borderie
l.borderie@evolucare.com0762879928

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026