Cervical spondylotic radiculopathy
Conditions
Interventions
trial group:Ultrasound-guided cervical nerve root block combined with dry needle therapy
control group:Ultrasound-guided cervical nerve root block
Sponsors
Affiliated Hospital of Xuzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Patients meeting CSR diagnostic criteria; 2.The curative effect of simple drug treatment was not satisfactory; 3.The course of the disease is less than or equal to 1 year; 4.Body Mass Index (BMI) ranged from 18.5 to 24 kg/m2 and aged 18 to 60 years; 5.Agree to participate in the study and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1.Abnormal or unstable cervical anatomy and other types of cervical spondylosis; 2.Patients with cervical spine tumor, tuberculosis, and osteomyelitis; 3.Exclude other causes of neck, shoulder, and upper limb pain; 4.Upper limb muscle strength <= 3 grades; 5.Patients with heart, lung, brain, blood system diseases and osteoporosis; 6.The treatment site has severe skin injury or skin disease; 7.Needle sickness or allergy to therapeutic drugs (lidocaine, hormone, Paracetamol, celecoxib, and Tramadol Hydrochloride Tablets); 8.During menstruation, pregnancy, or lactation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numerical rating scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Cervical Range of Motion;Neck Disability Index;Dosage and frequency of remedial drugs;Temperature change in pain area; | — |
Countries
China
Contacts
Public ContactYan Yuan
Department of Pain treatment, Affiliated Hospital of Xuzhou Medical University
Outcome results
None listed