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Construction and Validation of an AI-Assisted Diagnosis, Treatment, and Prognostic Evaluation Model for Acute Retinal Necrosis Syndrome (ARN)

Construction and Validation of an AI-Assisted Diagnosis, Treatment, and Prognostic Evaluation Model for Acute Retinal Necrosis Syndrome (ARN)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111128
Enrollment
Unknown
Registered
2025-10-27
Start date
2025-10-30
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Acute Retinal Necrosis Syndrome

Interventions

AI-Assisted Diagnosis and Treatment Group:Diagnostic stage: Input the patients clinical symptoms, fundus examination results, etiological detection data, etc. into the "Acute Retinal Necrosis Syndrome

Sponsors

Shanxi Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Jointly diagnosed by =2 fundus disease specialists with associate chief physician title, meeting internationally recognized ARN diagnostic criteria (referring to Takase H criteria 2015 and Uveitis Working Group criteria 2021), specifically satisfying at least 2 of the 3 core indicators: (1) peripheral retinal necrosis lesions, (2) occlusive retinal arteritis, (3) vitreous opacity, accompanied by positive HSV/VZV detection in intraocular fluid PCR or characteristic disease progression manifestations;? 2. Visited Shanxi Eye Hospital with baseline data including 23 core indicators (demographic characteristics, etiological typing, retinal vascular occlusion range, treatment plan, etc.), with key data missing rate <=5%;? 3. Informed consent obtained from patients or legal guardians, able to cooperate with = 3 months of follow-up to collect prognostic data such as retinal detachment and visual acuity changes;? 4. No restrictions on age or gender, including patients with monocular/binocular involvement, covering different disease severities (mild/moderate/severe) and etiological types (VZV/HSV infection) to ensure sample representativeness.

Exclusion criteria

Exclusion criteria: 1. Not meeting ARN diagnostic criteria, or diagnosed with confused diseases (e.g., CMV retinitis, toxoplasmic retinochoroiditis, proliferative diabetic retinopathy, etc.);? 2. Missing rate of core indicators (etiological results, treatment plan, visual acuity monitoring, etc.) >5%, which cannot be supplemented by clinical records;? 3. Complicated with severe heart/liver/kidney failure, advanced malignancy, etc., with expected survival < 3 months, or unable to cooperate with follow-up due to mental disorders;? 4. Previous ocular surgeries (except uncomplicated cataract surgery with good recovery) such as corneal transplantation and glaucoma filtration surgery, which may affect diagnosis, treatment and prognostic evaluation;? 5. Refusing to provide clinical data for model construction, or disagreeing to participate in follow-up and verification procedures.

Design outcomes

Primary

MeasureTime frame
Incidence of retinal detachment;Best Corrected Visual Acuity;Involvement of the second eye;Baseline characteristics (e.g., age, gender, affected eye);

Secondary

MeasureTime frame
Vitreous inflammation grading;Time from symptom onset to antiviral treatment;Comorbidity status;

Countries

China

Contacts

Public ContactZhang Yu

Shanxi Eye Hospital

2145962552@qq.com+86 351 828 6884

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026