Cervical myelopathy
Conditions
Interventions
control group:conventional perioperative care
experimental group:perioperative care of enhanced recovery
Sponsors
Fujian Medical University Union Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: (1) Aged 18 to 70 years old; (2) Preoperative MRI and CT confirmed signs of cervical disc herniation and compression of spinal cord; (3) Typical manifestations of cervical spondylosis, such as neck and shoulder pain, numbness of both upper limbs, weakened grip strength, and cotton feeling on the feet; (4) Normal conservative treatment for 3 months, no obvious relief or even worse symptoms; (5) No absolute surgical contraindication; (6) Informed consent of the patient.
Exclusion criteria
Exclusion criteria: (1) Pregnant or lactating women; (2) Patients with a history of cervical spine surgery; (3) Congenital spinal stenosis or cervical deformity; (4) Patients with dysphagia before surgery; (5) Patients with infection and tumor; (6) Those who fail to follow the follow-up required by the protocol, or the researcher believes that the participants' participation in the study will increase the risk; (7) Fail to provide written informed consent, or fail to follow the pilot program; (8) Those whose expected survival time is less than 1 year; (9) Persons with language communication disorder; (10) Participating in other clinical trials; (11) Patients with rheumatic immune diseases that may cause similar symptoms; (12) Not suitable for MRI, CT enhancement and other special examinations.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| KPS score;japanese orthopaedic association; | — |
Secondary
| Measure | Time frame |
|---|---|
| Numeric Rating Scale;Neck Disability Index; | — |
Countries
China
Contacts
Public ContactZhong Guiqin
Fujian Medical University Union Hospital
Outcome results
None listed