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Development and validation study of artificial intelligence fundus recognition technology for aid in the diagnosis of obstructive sleep apnea syndrome

Development and validation study of artificial intelligence fundus recognition technology for aid in the diagnosis of obstructive sleep apnea syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090555
Enrollment
Unknown
Registered
2024-10-08
Start date
2021-10-08
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

Obstructive sleep apnea syndrome

Interventions

Gold Standard:OSA diagnostic criteria: mainly based on medical history, physical signs and polysomnography (PSG) monitoring results. OSA can be diagnosed if there are typical clinical symptoms of noct
and/or minimum SaO2: mild 85-90%, moderate 80-<85%, severe <80%.
Index test:fundus photography

Sponsors

Sleep Medicine Center, Department of Psychiatric, Nanfang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Patients attending the Sleep Medicine Center of Nanfang Hospital of Southern Medical University for PSG monitoring who also met the following criteria: (2) Age =18 years old (3) Completed polysomnography with valid data (4) No history of eye trauma or retinal surgery (5) Able to cooperate in retinal examination (6) Fully informed about the content of the study and signed an informed consent form

Exclusion criteria

Exclusion criteria: (1) Those who suffer from major diseases such as malignant tumors, liver or kidney insufficiency, or blood system diseases (2) Those with congenital diseases or psychiatric disorders, or those with impaired consciousness who are unable to cooperate with the program (3) Fundus photographs whose overall quality of image acquisition is so poorly assessed and credible that feature extraction and analysis cannot be performed

Design outcomes

Primary

MeasureTime frame
Apnea-Hypopnea Index (AHI);

Countries

China

Contacts

Public ContactYuan Feng

Sleep Medicine Center, Department of Psychiatric, Nanfang Hospital, Southern Medical University

yuanstar@126.com+86 138 2502 7946

Outcome results

None listed

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