post-operative axial symptoms after posterior cervical surgery
Conditions
Interventions
Control Group:Injection of 2cm paracupoint
Experimental Group:acupoint injection
Sponsors
No.905 Hospital of PLA Navy Shanghai China
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Those who meet the following 5 items can be included in the study. If there is any inconformity the patient cannot enter the study 1.Patients who have undergone posterior cervical single-door decompression surgery 2.Cervical VAS score of =6 aged 3.Between 18 and 80 years 4.Meet the Takeuchi criteria for the diagnosis of post-operative axial symptoms (AS) 5.Patients agree to participate in this study and cooperate in communication.
Exclusion criteria
Exclusion criteria: Patients cannot enter the study if any of the following are met: 1.Patients with a history of cervical spine surgery; 2.Pregnant women; 3.Patients with cervical spine infections conditions; 4.Patients with comorbid neurological or psychological disorders such as anxiety depression insomnia or a history of tumors; 5.Patients older than 80 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| "effective" patient rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in AS grading;Accompanying symptoms during pain: stiffness, heaviness;Changes in VAS scores;Oral intake of non-steroidal anti-inflammatory drugs (NSAIDs) and their quantity; | — |
Countries
china
Contacts
Public Contactwenchao zhou
No.905 Hospital of PLA Navy Shanghai China
Outcome results
None listed