- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07707856
AI Prediction of Treatment Response in DME
Artificial Intelligence and Imaging Biomarkers for Predicting Treatment Response in Diabetic Macular Edema: A Systematic Review
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Diabetic macular edema is one of the most common causes of visual impairment in patients with diabetic retinopathy. Despite the widespread use of intravitreal anti-VEGF agents, corticosteroids, laser photocoagulation, and combination therapies, individual responses remain highly variable. Early identification of patients who are likely to respond to specific treatments may improve visual outcomes while reducing unnecessary treatment burden.
Advances in retinal imaging, particularly optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA), have enabled detailed characterization of retinal structural and vascular biomarkers associated with treatment outcomes. Commonly investigated biomarkers include central retinal thickness, intraretinal cysts, subretinal fluid, hyperreflective retinal foci, disorganization of the retinal inner layers (DRIL), ellipsoid zone integrity, external limiting membrane integrity, choroidal thickness, choroidal vascularity index, retinal fluid volume, vascular density, and foveal avascular zone parameters.
Artificial intelligence techniques, including conventional machine learning and deep learning algorithms, increasingly integrate retinal imaging features with demographic and clinical variables to predict functional and anatomical responses to therapy. Reported prediction models have demonstrated promising diagnostic performance, although considerable variability exists regarding imaging modalities, model architecture, validation strategies, outcome definitions, and reporting standards.
This systematic review will comprehensively evaluate published studies investigating AI-based prediction of treatment response in patients with diabetic macular edema. The review will identify imaging biomarkers contributing to predictive performance, compare machine learning and deep learning approaches, evaluate different retinal imaging modalities, summarize reported model performance metrics including area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, specificity, and F1-score, and assess methodological quality using validated risk-of-bias assessment tools. Where sufficient homogeneous data are available, a random-effects meta-analysis will be conducted to quantitatively synthesize model performance.
The findings are expected to identify robust imaging biomarkers, highlight current limitations of AI prediction models, and provide recommendations for future research and clinical implementation of AI-assisted precision medicine in diabetic macular edema.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Benha
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Banhā, Benha, Egypt, 13111
- Benha University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults aged 18 years or older.
- Diagnosis of diabetic macular edema (DME) confirmed by clinical examination and optical coherence tomography (OCT).
- Treatment with intravitreal anti-vascular endothelial growth factor (anti-VEGF), intravitreal corticosteroids, focal/grid laser photocoagulation, or combination therapy.
- Availability of baseline retinal imaging, including OCT, OCT angiography (OCTA), fundus photography, or multimodal imaging suitable for artificial intelligence analysis.
- Availability of baseline and follow-up best-corrected visual acuity (BCVA) and central retinal thickness (CRT) measurements.
- Complete demographic and clinical data required for model development or validation.
- Minimum follow-up of 3 months after initiation of treatment.
Exclusion Criteria:
- Macular edema due to causes other than diabetes.
- Previous vitreoretinal surgery in the study eye.
- Coexisting retinal diseases that may affect visual or anatomical outcomes (e.g., retinal vein occlusion, age-related macular degeneration, uveitis, inherited retinal disorders).
- Significant media opacity resulting in poor-quality retinal imaging.
- Incomplete clinical records or missing imaging data.
- Follow-up duration less than 3 months.
- Images that fail quality-control criteria for artificial intelligence analysis.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Artificial Intelligence
This review focuses on published studies evaluating artificial intelligence (AI)-based models that use retinal imaging biomarkers to predict treatment response in patients with diabetic macular edema.
The review synthesizes evidence on machine learning and deep learning approaches, imaging modalities including optical coherence tomography (OCT), optical coherence tomography angiography (OCTA), and fundus photography, and their reported predictive performance for anatomical and functional treatment outcomes.
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Participants undergo retinal imaging analysis using artificial intelligence-based prediction models developed from optical coherence tomography (OCT), optical coherence tomography angiography (OCTA), fundus photography, and relevant clinical variables.
The AI algorithms are used to predict treatment response in diabetic macular edema, including anatomical and functional outcomes following anti-vascular endothelial growth factor (anti-VEGF), corticosteroid, laser, or combination therapies.
The AI analysis does not alter clinical management and is performed for predictive evaluation only.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Predictive Performance of the Artificial Intelligence Model for Treatment Response
Time Frame: Baseline to 12 months
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To evaluate the ability of the artificial intelligence model to predict treatment response in patients with diabetic macular edema using retinal imaging biomarkers.
Model performance will be assessed using the area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, specificity, precision, recall, F1-score, and calibration, where applicable.
|
Baseline to 12 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Central Retinal Thickness
Time Frame: Baseline to 12 months
|
Reduction in central retinal thickness measured by optical coherence tomography and its relationship with AI prediction results.
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Baseline to 12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AI-DME-SR-2026
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Diabetic Retinopathy
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Sara A BelalRecruitingDiabetes (DM) | Diabetic Retinopathy (DR) | Retinopathy, Diabetic | Diabetic Retinopathy Associated With Type 2 Diabetes MellitusEgypt
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