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RecruitingNCT07424755Updated Feb 20, 2026

AI-Empowered Fundus Platform

An observational study in High Myopia, sponsored by Shanghai 10th People's Hospital. Recruiting at 1 site in China. Per ClinicalTrials.gov, last updated 2026-02-20.

Sponsored by Shanghai 10th People's Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Mar 2026, 7 months ago, but the record still lists the study as recruiting.
  • Started Oct 2024; still recruiting 2 years later.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
1,000
Sex
All
01

Study summary

According to estimates by the World Health Organization, approximately half of the global adult population currently suffers from varying degrees of myopia. In urban areas of China, the myopia rate among primary school students has reached about 40%, and can exceed 80% in high school students. The proportion of patients with high myopia (refractive error greater than 600 degrees) is also increasing year by year. This group is more prone to severe visual problems, including an increased risk of complications such as cataracts, glaucoma, and macular degeneration. Pathological myopia is the main risk factor for vision loss caused by high myopia. In such patients, the elongation of the ocular axis leads to local thinning and protrusion of the posterior pole of the eyeball, forming a posterior scleral staphyloma. Posterior scleral staphyloma is the most representative pathological feature of pathological myopia. Local dilation of the choroid leads to thinning and stretching of the retina, which may ultimately cause problems such as macular retinal schisis, seriously affecting vision and even leading to blindness.

This project aims to develop a multimodal intelligent screening system by combining the excellent imaging technology and advanced artificial intelligence (AI) of the Optos non-mydriatic ultra-wide-angle laser scanning ophthalmoscope, B-scan ultrasonography ophthalmic diagnostic instrument, and optical coherence tomography (OCT). The system is designed to achieve precise identification and assessment of ocular fundus diseases, especially pathological myopia, and particularly the core condition of posterior scleral staphyloma (PSS). Simultaneously, a vision prediction model will be constructed to assist doctors in formulating personalized diagnosis and treatment strategies, predicting the trend of vision deterioration, and enhancing the effectiveness of early intervention. This system is expected to significantly improve the prevention and control of pathological myopia, reduce the risk of blindness, and play a pivotal role in telemedicine services, benefiting people in remote areas and promoting public health equity and service quality.

02

Conditions studied

  • High Myopia
03

In context

Lead sponsor

Shanghai 10th People's Hospital is the lead sponsor of 167 studies on the registry; 45 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

This retrospective study enrolled patients diagnosed with high myopia and posterior staphyloma (PSS) who visited the Department of Ophthalmology, Shanghai Tenth People's Hospital before October 2024.

Sample Size:A total of 1,000 patients (600 for training, 200 for validation, and 200 for internal testing) from the hospital cohort, contributing approximately 6,000 multimodal images.

Inclusion criteria

Patients with a diagnosis of cataract and high myopia and posterior staphyloma, who underwent comprehensive ophthalmic examinations including ultra-widefield fundus photography (Optos), B-scan ultrasonography, and optical coherence tomography (OCT). Baseline data, including demographics, health status, ophthalmic history, and ocular biometric parameters, were completely documented.

Exclusion criteria

Exclusion Criteria:

Patients with poor-quality images affecting PSS identification, severe coexisting ocular diseases including glaucoma, diabetic retinopathy that cause media opacities, or severe systemic diseases that could interfere with the study outcomes.

05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
1,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Cataract patients with posterior staphyloma due to high myopia

    Diagnostic Test: Multimodal Ocular Imaging and Biometry with Aritifical Intelligence Analysis

Interventions

  • Diagnostic testMultimodal Ocular Imaging and Biometry with Aritifical Intelligence Analysis

    The patient underwent a complete set of fundus color photography, B-scan ultrasonography, and OCT imaging during the consultation, and preoperative baseline data, including demographic information, health status, ophthalmic history, and ocular biometric parameters, were collected and recorded in detail

06

What researchers measure

Primary outcomes

  1. Data collection outcome

    Demographic data clasification of posterior scleral staphyloma visual acuity and imaging data

    Time frame: From October 2024 to April 2026 (Data collection from patients who visited the hospital before October 2024)

Secondary outcomes

  1. AI modeling Analysis

    Diagnostic performance of the AI model for posterior scleral staphyloma. Area under the receiver operating characteristic curve (AUC-ROC) of the AI model. Accuracy, sensitivity, and specificity of the model in detecting posterior scleral staphyloma. Comparison of AI performance and doctors' performance

    Time frame: From April 2026 to October 2026

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Study locations

1 of 1 sites recruiting
  • Shanghai 10th People's Hospital
    Shanghai, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07424755
Lead sponsor
Shanghai 10th People's Hospital
Responsible party
Sun Yilin (Resident Physician, Shanghai 10th People's Hospital) — Principal investigator
First posted
Feb 20, 2026
Start date
Oct 1, 2024
Primary completion
Mar 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Feb 20, 2026

Study contacts

yiwen Hu
Contact
1006108590@qq.com
+86 18019320181

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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