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Construct an intelligent diagnosis system for sleep apnea hypopnea syndrome

Construct an intelligent diagnosis system for sleep apnea hypopnea syndrome

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069223
Enrollment
Unknown
Registered
2023-03-09
Start date
2023-03-15
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

obstructive sleep apnea hypopnea syndrome, OSA

Interventions

Modeling group:NONE
Test group:NONE

Sponsors

Eye & ENT Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. High school degree or above; 2. OSA adult males aged 18-65 years (AHI >= 5 times/hour); 3. BMI<32kg/m^2; 4. No history of OSAS treatment; 5. No visual impairment (normal vision or corrected to normal); 6. Right-handed;

Exclusion criteria

Exclusion criteria: 1. Dementia, cerebrovascular disease, history of brain trauma, chronic respiratory disease; 2. Other primary sleep disorders; 3. Combined mental disorders (including depression, anxiety, alcoholism and other drug addictions); 4. Other serious systemic and organ diseases with non-OSA comorbidities such as tumors; 5. OSA patients who had undergone surgery and drug therapy; 6. Routine use of psychiatric system, anti-anxiety and depression drugs or drugs that can cause sleep structure disorders; 7. Non-osa induced daytime sleepiness; 8. Associated with congenital or acquired craniofacial malformations such as Crouzon, Apert, Treacher-Collins, Robin sequence, Down syndrome, etc.; 9. Performed craniofacial surgery (including orthodontic surgery, plastic surgery, orthodontic).

Design outcomes

Primary

MeasureTime frame
polysomnography;alertness test system;face and neck recognition system;

Countries

China

Contacts

Public ContactWei Chunsheng, Huang Jingjing

Eye & ENT Hospital of Fudan University

gennie_xuan@163.com+86 13701740606

Outcome results

None listed

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