Cervical degenerative disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. The patient is between the ages of 18 and 80, regardless of gender, and is willing to sign an informed consent form; 2. All patients' clinical manifestations are consistent with their imaging features; 3. Conservative treatment for more than 3 months is ineffective, and single door surgery is planned for treatment.
Exclusion criteria
Exclusion criteria: 1. Individuals with a history of cervical trauma or cervical surgery; 2. Patients with combined spinal deformities, tumors, infections, and thoracolumbar spinal cord nerve compression; 3. Congenital cervical fusion and other developmental abnormalities; 4. Malignant tumor patients; 5. Poor physical condition and inability to tolerate surgery; 6. Patients (or their guardians) with cognitive impairment who cannot provide sufficient informed consent; 7. Patients who have participated in other clinical trials within the past month; 8.Patients with active tuberculosis, cytomegalovirus, severe fungal infection, or HIV infection; 9. Elderly patients with osteoporosis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Radiological examination;Clinical function evaluation;Visual Analogue Scale (VAS), used to assess the severity of cervical spine and upper limb pain.;Neck Disability Index (NDI), used to assess the impact of neck pain on daily living function.;Modified Japanese Orthopaedic Association Score (mJOA), used to assess spinal cord functional status.;36-Item Short Form Health Survey (SF-36), a quality of daily life assessment scale.; | — |
Secondary
| Measure | Time frame |
|---|---|
| Laboratory inspections;Condition during perioperative period; | — |
Countries
China
Contacts
Affiliated Hospital of Chifeng University