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Clinical Trials/NCT07643129
NCT07643129Not yet recruitingNot Applicable

Clinical Utility of an Artificial Intelligence-Assisted Lesion-Based Urgent Referral Triage System for Ultra-Widefield Retinal Images: A Prospective Multi-Reader Multi-Case Randomized Reader Study

Xiamen Ophthalmology Center Affiliated to Xiamen University0 sites8 target enrollmentStarted: June 15, 2026Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
8

Study Overview

Brief Summary

his study evaluates the clinical utility of an artificial intelligence (AI)-assisted lesion-based urgent referral triage system for ultra-widefield (UWF) retinal images.

Unlike disease-classification systems, the AI system identifies predefined vision-threatening retinal findings and generates lesion-level urgent referral recommendations. Participating ophthalmologists will evaluate UWF retinal images under randomized AI-assisted and unassisted conditions.

The primary objective is to determine whether lesion-based AI assistance improves urgent referral triage performance compared with unaided image interpretation.

Detailed Description

Ultra-widefield retinal imaging is increasingly used for retinal disease screening and referral triage. Many vision-threatening retinal abnormalities require timely identification and referral to retinal specialists.

The AI system evaluated in this study is designed as a lesion-based triage tool rather than a disease-diagnosis system. The model identifies predefined urgent referral retinal findings and generates referral recommendations based on lesion-level evidence.

Urgent referral findings include:

  • Retinal detachment
  • Untreated retinal tear or retinal hole
  • Vitreous hemorrhage
  • Pre-retinal hemorrhage
  • Subretinal hemorrhage
  • Retinal neovascularization
  • Optic disc neovascularization
  • Tractional fibrovascular membrane Treated retinal tears associated with laser barricade scars are classified as non-urgent referral findings.

A total of 600 UWF retinal images acquired using Zeiss and Optos imaging systems will be included.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Licensed ophthalmologists
  • Willing to participate as readers
  • Completion of study training

Exclusion Criteria

  • Retinal specialists involved in establishing gold-standard labels
  • Prior access to gold-standard labels
  • Incomplete study participation

Investigators

Sponsor
Xiamen Ophthalmology Center Affiliated to Xiamen University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

XiujuChen

Investigator

Xiamen Ophthalmology Center Affiliated to Xiamen University

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