cervical spondylosis
Conditions
Interventions
Experimental group1:Zero-P
Experimental group2:plate-cage
Sponsors
Tongji Hospital of Shanghai
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients who can be clearly diagnosed as cervical spondylosis based on symptoms, signs, and imaging examinations; 2. Patients who are ineffective after conservative treatment, seriously affect their life and work, and require surgical treatment; 3. No gender limit, aged 18 to 80 years; 4. Patients who agree to surgery and regular follow-up visits and who can meet the needs of this study; 5. Those who agree to sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients suffering from severe posterior longitudinal ligament ossification or severe osteoporosis; 2. Patients with Diffuse Idiopathic Skeletal Hyperostosis (Diffuse Idiopathic Skeletal Hyperostosis, DISH) and Ankylosing Spondylitis (AS); 3. Patients who have undergone severe degeneration in the adjacent segments of the preoperative responsible segment; 4. Patients with severe complications before surgery; 5. Patients with chronic cardiovascular and cerebrovascular diseases such as myocardial infarction, cerebral infarction and cerebral hemorrhage 6. Patients with a history of cervical spine surgery; 7. Metal allergy, allergic physique or allergy to multiple drugs; 8. Accompanied by spinal tumors or infections and other diseases; 9. Have severe bleeding tendency or coagulation dysfunction; 10. Pregnant or lactating women and those who are contraindicated in imaging examinations; 11. Mental or cognitive impairment; 12. The researcher believes that it is inappropriate to participate in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain visual analog scale;Cervical curvature; | — |
Countries
China
Contacts
Public ContactYu Yan
Tongji Hospital of Shanghai
Outcome results
None listed