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Research on Intelligent Assessment of Facial Nerve Palsy Based on AI ”Visual Recognition“

Research on Intelligent Assessment of Facial Nerve Palsy Based on AI ”Visual Recognition“

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119608
Enrollment
Unknown
Registered
2026-02-28
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Peripheral facial nerve palsy

Interventions

Facial nerve palsy group:Static symmetry analysis,Dynamic function assessment
Non-facial paralysis group:Static symmetry analysis,Dynamic function assessment

Sponsors

Zhejiang Provincial Hospital of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: Facial nerve palsy group 1. Meet the diagnostic criteria of peripheral facial nerve palsy. 2. Between 16 and 65 years of age (including 16 and 65 years of age), regardless of gender. 3. Patients with complete frontal head images. 4. Able to cooperate in completing the questionnaire and physical examination. 5. Patients who agreed to participate in image acquisition and signed the informed consent form. Non-facial palsy group 1. Patients with symmetrical facial movements on both sides. 2. No history of peripheral facial paralysis, central facial paralysis or extraocular muscle paralysis. 3. Able to cooperate in completing the questionnaire and physical examination. 4. Patients who agreed to participate in image acquisition and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with facial anatomical structure defects caused by various diseases. 2.Patients with facial anatomical asymmetry due to congenital hypoplasia. 3.Patients with altered positions of facial anatomical structures caused by makeup or other factors. 4.Patients wearing additional items on the face, such as glasses, nasogastric tubes, or medical dressings. 5.Patients with facial defects, prominences, scars, or asymmetric movement(not attributable to this disease). 6.Patients whose images were not acquired usingthe specified image acquisition equipment. 7.Pregnant or lactating women, and individuals with a known hypersensitivity to the image acquisition process. 8.Patients with severe primary diseases such as cardiovascular, cerebrovascular, hepatic, renal, or hematopoietic system disorders, as well as patients with psychiatric illness. 9.Individuals currently participating in other clinical studies.

Design outcomes

Primary

MeasureTime frame
dynamic function assessment;AI-based quantitative analysis and early warning;static symmetry analysis;

Countries

China

Contacts

Public ContactWeijing Zhan

Zhejiang Provincial Hospital of TCM

zwj_ea@163.com+86 571 87071756

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026