Construction and validation of the surgical outcomes and postoperative complications prediction model for cervical spinal cord injury based on radiomics: a prospective cohort study

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400082514

Enrollment

Unknown

Registered

2024-03-31

Start date

2024-04-01

Completion date

Unknown

Last updated

2024-04-08

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

Conditions

cervical spinal cord injury

Interventions

Observation group:NA

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1)Age 18-80 years old; (2) All patients were diagnosed with cervical spinal cord injury through medical history, physical examination and imaging examination (X-ray, CT, MRI); (3) Those who agree to sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1)Incomplete information; (2) Patients with contraindications for X-ray, CT and MRI scanning; (3) lactating and pregnant women; (4)Patients who cannot cooperate with the relevant examination of this project and do not agree to sign the informed consent form.

Design outcomes

Primary

Measure	Time frame
Clinical function evaluation;	—

Secondary

Measure	Time frame
Dysphagia;C5 nerve root paralysis;Imageological examination;Colligation condition during operation;laboratory inspections;	—

Countries

China

Contacts

Public ContactDacheng Sang

The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College)

dachengsang1616@163.com+86 134 2616 0593

Outcome results

None listed

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