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Multi-modal Imaging and Artificial Intelligence Diagnostic System for Multi-level Clinical Application

Multi-modal Imaging and Artificial Intelligence Diagnostic System for Multi-level Clinical Application

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03899623
Enrollment
3000
Registered
2019-04-02
Start date
2018-04-23
Completion date
2019-12-31
Last updated
2019-04-02

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

Conditions

Diabete Mellitus, Diabetic Retinopathy

Keywords

Diabete Mellitus, Diabetic Retinopathy, Artificial Intelligence

Brief summary

This study is to build an multi-modal artificial intelligence ophthalmological imaging diagnostic system covering multi-level medical institutions. We are going to evaluate this system in an evidence-based medicine view, taking diabetic retinopathy as an example. And clinical diagnostic criteria will be made based on this multi-modal artificial intelligence imaging diagnostic system. The study is designed as a cross-sectional study involving 1,000 normal individuals, 1,000 diabetes patients without ocular complications, and 1,000 with diabetic ocular complications. Statistical analysis of the diagnostic sensitivity and specificity of the artificial intelligence system will be made, and ROC curve wil be draw.

Interventions

None listed

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-sen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

Group A(normal individuals): Meet all the items 1 \ 5 below 1. No familial or hereditary retinopathy; 2. No history of ocular trauma and / or history of ocular disease (except for mild to moderate refractive errors and / or age-related cataracts); 3. No drug use history that may cause side effects of retina (such as chloroquine, hydroxychloroquine, chlorpromazine, rifampin, etc.); 4 binocular diopter ≤ ± 6.00D; No systemic diseases that may affect the retina. Group B(diabetes patients without ocular complications): meet any of 1 to 3, and both 4 to 5 items 1. Diagnosed with type 1 diabetes for more than 5 years; 2. Diagnosed with type 2 diabetes patients; 3. Diagnosis of gestational diabetes patients; 4. Without systemic disease that may affect the retina except for diabetes; 5. Meet the standards of 1 to 4 items. Group C(patients with diabetic ocular complications): meet with any of 1 to 3, and all 4 to 6 items 1. Diagnosed with type 1 diabetes for more than 5 years; 2. Diagnosed with type 2 diabetes patients; 3. Diagnosis of gestational diabetes patients; 4. Meet the guidelines for diagnosis and treatment of diabetic retinopathy in any stage of diabetic retinopathy and / or diabetic macular edema. 5. Without systemic disease that may affect the retina except for diabetes; 6. A group to meet the criteria for 1 to 4 items.

Exclusion criteria

1. Refractive pathway is turbid, so that fundus image can not be clearly photographed; 2. With other fundus diseases and / or other diseases that seriously affect the visual function; 3. Any eye infection, such as conjunctivitis, keratitis, scleritis, endophthalmitis, acute and chronic dacryocystitis, or eye injury; 4. Serious systemic diseases such as diabetes, hypertension, heart failur,renal failure; 5. Can not cooperate with the examiner due to mental or other reasons.

Design outcomes

Primary

MeasureTime frameDescription
The diagnostic sensitivity, specificity and ROC curve of the artificial intelligence(AI) system compared with reference standard (ophthalmologist).It will take 15~20min for each subject to take the exams.Sensitivity: the percentage of diabetic retinopathy(DR) patients who are correctly identified as having the condition by AI. Sensitivity=True positive/(True positive+False negative). Specificity: the percentage of healthy people who are correctly identified as not having the condition by AI. Specificity=True negative /(True negative +False positive). The ROC curve was plotted with true positive rate (sensitivity) as the ordinate and false positive rate (1-specificity) as the abscissa.

Countries

China

Contacts

Primary ContactYuan Jin, Professor
yuanjincornea@126.com8602087333391

Outcome results

None listed

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