Clinical Evaluation of VeriSee AMD in Screening for Age-Related Macular Degeneration

Sponsor
Acer Medical Inc. (Industry)
Overall Status
Completed
CT.gov ID
NCT05593913
Collaborator
National Taiwan University Hospital (Other)
986
1
6.7
146.4

Study Details

Study Description

Brief Summary

An observational study is designed to evaluate the clinical performance of VeriSee AMD for potential age-related macular degeneration (AMD) screening from color fundus photography images. The sensitivity and specificity of VeriSee AMD's automated image analysis for screening AMD will be determined through the comparison with the gold standard, which is the judgment of AMD by the ophthalmologists.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This is a retrospective, single-center, observational study to assess the clinical performance of VeriSee AMD in screening for potential age-related macular degeneration (AMD).

    Potential subjects with images of color fundus photography will be selected for eligibility, and then the ophthalmologist further confirms the images with legible quality. Three independent ophthalmologists (or evaluators) having more than 6 years of experience in retina will evaluate AMD from the color fundus photography images with different sequences of images independently. These three evaluators are different from the ophthalmologist who is responsible for deciding subject's eligibility. The evaluators determine the severity of AMD based on the four-level scale which is the AMD Severity Scale stated in Age-Related Eye Disease Study (AREDS) Report No. 6. Before the study, the training section is necessary to ensure the consensus of the AMD severity grading among three evaluators. The severity determined by the majority of the grade the three evaluators gave is considered the gold/reference standard in this study. Therefore, level 1 and level 2 are classified as non-mtl3AMD, while level 3 and advanced AMD (level 4) are classified as mtl3AMD. The clinical performance displayed as sensitivity and specificity will be determined by comparing the AMD results between VeriSee AMD and the gold standard.

    VeriSee AMD is intended to screen AMD from the images taken by color fundus photography, which can assist the physicians to assess whether further examination for retinopathy by the ophthalmologist is needed. The screening result of AMD will be non-mtl3AMD or mtl3AMD for the physicians' reference and does not intend to diagnose AMD, detect concomitant diseases, or treat AMD.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    986 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    A Single-center, Retrospective Study to Evaluate the Clinical Performance of Artificial Intelligence Medical Assisted Diagnostic Software (VeriSee AMD) for Screening of Age-Related Macular Degeneration
    Actual Study Start Date :
    Jan 17, 2022
    Actual Primary Completion Date :
    Mar 3, 2022
    Actual Study Completion Date :
    Aug 10, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Specificity [1 day]

      To evaluate the clinical performance of VeriSee DR by determining the Specificity. Specificity = 100% x TN/(TN+FP)

    2. Sensitivity [1 day]

      To evaluate the clinical performance of VeriSee DR by determining the sensitivity. Sensitivity = 100% x TP/(TP+FN)

    Secondary Outcome Measures

    1. Positive Predictive Values (PPV) [1 day]

      To evaluate the clinical performance of VeriSee AMD by determining the positive predictive values (PPV). Positive predictive value (PPV) =100% x TP/(TP+FP)

    2. Negative Predictive Values (NPV) [1 day]

      To evaluate the clinical performance of VeriSee DR by determining the negative predictive values (NPV). Negative predictive value (NPV) = 100% x TN/(FN+TN)

    3. The percentage of subjects' images with insufficient quality as judged by VeriSee AMD [1 day]

      The percentage of the images with insufficient quality as determined by VeriSee AMD will be presented.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Subject with age ≥ 50 years old

    • Subject with image taken by color fundus photography that meet the following requirement:

    1. The resolution of image is 271x271 pixels or higher;

    2. The angle view of image is 45 or 50 degree.

    • Subject's image includes macula as judged by the ophthalmologist.
    Exclusion Criteria:
    • The color fundus photography image previously used by VeriSee AMD during the development process and pre-clinical test

    • The macula or other part in the image of color fundus photography is unclear to determine the disease condition as judged by the ophthalmologist.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Taiwan University Hospital Taipei Taiwan 100

    Sponsors and Collaborators

    • Acer Medical Inc.
    • National Taiwan University Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Acer Medical Inc.
    ClinicalTrials.gov Identifier:
    NCT05593913
    Other Study ID Numbers:
    • AHCI21001
    First Posted:
    Oct 26, 2022
    Last Update Posted:
    Oct 26, 2022
    Last Verified:
    Oct 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 26, 2022