Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07243665

Glaucoma Screening Using Artificial Intelligence Assisted Clinical Model in Singapore's Diabetic Eye Screening Program

Glaucoma is major cause of irreversible blindness and is characterized by optic nerve damage and visual field loss. Screening for glaucoma is challenging due to lack of a simple, accurate, cost-efficient and standardized process. Artificial intelligence, (AI) especially deep learning (DL) algorithms have potential to automate glaucoma detection, but have to be evaluated in real world settings, before public deployment. This study aims to evaluate the screening accuracy of a DL algorithm for glaucoma detection using colour fundus photographs (CFP) in a pragmatic randomised control trial (RCT). The algorithm will be tested in 1040 eligible patients with diabetes, recruited from the Diabetes & Metabolism Centre's clinics under the Singapore Integrated Diabetic Retinopathy Program (SiDRP) and randomized to 2 arms: AI-assisted model vs current standard of care (grader assessment). The performance of both arms will be compared to performance of study ophthalmologist in diagnosing glaucoma. We hypothesize that the DL model has better screening performance in detecting glaucoma in the community, compared to the current practice method.

Recruiting

Interested in participating?

Request Info

Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Singapore National Eye Centre

Singapore, 168751

Location status: Recruiting

Location contact

Ching-Yu Cheng, MD, PhD

CONTACT

65767277

Hong Chang Tan

PRINCIPAL_INVESTIGATOR

Lavanya Raghavan

SUB_INVESTIGATOR

Lavanya Raghavan, MD

CONTACT

65767201

Shiwaza Aminath Moosa

PRINCIPAL_INVESTIGATOR

About this study

Background: Glaucoma is the leading cause of irreversible blindness worldwide, characterized by optic nerve damage and visual field loss. Screening for glaucoma remains challenging due to lack of a simple, standardized, and cost-effective test. Artificial intelligence (AI), especially deep learning (DL), offers potential to improve and standardize glaucoma detection. However, its performance must be prospectively validated in real-world settings before public deployment.

Aim: To evaluate the accuracy and cost-effectiveness of a DL algorithm using colour fundus photographs (CFP) as a clinical decision support tool for glaucoma detection in a real-world setting.

Methods: A two-centre, single-blind, pragmatic randomized controlled trial (RCT) will be conducted among 1,040 adults with diabetes recruited from the Diabetes & Metabolism Centre (DMC) and SingHealth Polyclinics-Bukit Merah under the Singapore Integrated Diabetic Retinopathy Programme (SiDRP). After fundus imaging, participants will be randomized 1:1 to AI-assisted grading or current manual grading by graders at the SiDRP reading center (520 subjects per arm). Diagnostic performance will be compared against the gold-standard glaucoma diagnosis, determined via comprehensive ocular examination including intraocular pressure measurement, visual field testing, optical coherence tomography, and dilated fundus assessment. Cost-effectiveness will be evaluated using a cohort-based Markov model to estimate lifetime costs and incremental cost-effectiveness ratios (ICERs) of the two glaucoma screening strategies.

Clinical Significance: Integrating AI into glaucoma screening can address resource constraints and streamline detection. This study will provide real-world evidence on the accuracy and cost-effectiveness of AI-based screening. If validated, it could be integrated into national screening programs to enhance early detection, reduce unnecessary referrals, and prevent avoidable blindness through a cost-efficient, scalable approach.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

We aim to recruit all eligible patients who attend Singapore General Hospital (SGH) Diabetes & Metabolism Centre's (DMC) clinics and SingHealth Polyclinics (SHP)-Bukit Merah under the Singapore Integrated Diabetic Retinopathy Programme (SiDRP). Patients are eligible for the study if

  • Aged 21 years old and above, with diabetes, including type 1 and type 2,
  • Retinal photos of the patients can be taken with the fundus camera in the clinics, regardless of photos' quality, and
  • They are willing and capable of providing a written informed consent form.

Exclusion criteria

Patients meeting any of the exclusion criteria will be excluded from participation:

  • Patients who have difficulty in having retinal photos taken or have difficulties in completing the ocular examination protocols according to investigator's decision.
  • Any other contraindication(s) as indicated by the endocrinologists responsible for the patients.

-

Treatment and study plan

Artificial Intelligence model to detect glaucoma

Diagnostic Test

A Vision Transformer model to detect glaucoma from fundus photos

Other names: Deep learning model, Vision Transformer, RetiGON

No intervention

Other

Control group with current practice model by human graders

Other names: Control group, Current practice model

Primary outcomes

  1. Evaluation of model performance

    Time frame: At study completion (after all fundus images have been graded and data collection is finalized; approximately within 12 months of study initiation)

    To compare the model performance in accuracy, sensitivity, specificity, positive predictive value and negative predictive value between the new AI-assisted clinical model and the current practice model in detecting glaucoma, with reference to the expert panel's standards.

Secondary outcomes

  1. Evaluation of time efficiency

    Time frame: At study completion (after all fundus images have been graded and data collection is finalized; approximately within 12 months of study initiation)

    To compare time efficiency between the AI-assisted clinical model and the current practice model, defined as the total time (in seconds) taken per participant for the entire screening process, from image access to final grading decision, recorded in real time during the grading session.

  2. Evaluation of Grader's Acceptance

    Time frame: At study completion (after all fundus images have been graded and data collection is finalized; approximately within 12 months of study initiation)

    To assess graders' acceptance and satisfaction with the AI-assisted clinical model compared to the current practice model in detecting glaucoma. Assessment will be conducted through brief in-task prompts during the grading process and through a structured post-study questionnaire.

Study contacts

Contact information is provided by the study sponsor or research team.

Ching-Yu Cheng, MD, PhD

CONTACT

[email protected]

65767277

Lavanya Raghavan, MD

CONTACT

[email protected]

65767201

Sponsors and collaborators

Lead sponsor

Singapore Eye Research Institute

Other

Collaborators

  • SingHealth Polyclinics
  • Singapore General Hospital

Registry information

Official study title

A Pragmatic Randomized Controlled Trial of a New Artificial Intelligence-Assisted Clinical Model in Opportunistic Screening for Glaucoma in the Singapore Integrated Diabetic Retinopathy Program

Acronym: AIGS

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Nov 24, 2025
Registry last updated
Jan 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.