Healthy or Cervical spondylotic radiculopathy
Conditions
Interventions
Cervical rotatory manipulation with crack sounds(Cervical spondylotic radiculopathy):Cervical rotatory manipulation with crack sounds
Cervical rotatory manipulation with crack sounds(Healthy):Cervical rotatory manipulation without crack sounds
Cervical rotatory manipulation without crack sounds(Healthy):Cervical rotatory manipulation without crack sounds
Cervical rotatory manipulation without crack sounds(Cervical spondylotic radiculopathy):Cervical rotatory manipulation without crack sounds
Sponsors
Guangzhou Medical University Affiliated Hospital of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Subjects with Cervical spondylotic radiculopathy: voluntarily sign informed consent; Age 18-45 years old; According to the Expert Consensus on the Standardized Diagnosis and Treatment of Cervical radiculopathy typical symptoms of root compression X-ray or CT examination showed changes of cervical disc herniation such as cervical joint hyperplasia vertebral space stenosis etc. MRI showed positive nerve root compression brachial plexus pull test or foraminal test and the patient was diagnosed as cervical radiculopathy. No recent inflammation and infection and no different types of arthritis; Willing to participate in this study. Healthy subjects: sign informed consent voluntarily; Age 18-45 years old; Healthy subjects were judged by the Expert Consensus on Management of Healthy Subjects/Participants in Phase I /BE clinical Trials; Willing to participate in this study.
Exclusion criteria
Exclusion criteria: Subjects of Cervical spondylotic radiculopathy: patients with myelopathy liver and kidney diseases cardiovascular and cerebrovascular diseases and respiratory diseases; Patients with blood disease diabetes autoimmune disease tumor disease; Patients with other types of cervical spondylosis; Accompanied by mental illness or cognitive impairment; Combined with cervical spinal stenosis; Rule out other types of disease manifested by upper limb pain; Subjects judged by the investigator to be unsuitable for participation in this study. Healthy subjects: with psychiatric or cognitive impairment; Subjects judged by the investigator to be unsuitable for participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| resting state electroencephalogram; | — |
Secondary
| Measure | Time frame |
|---|---|
| International positive and negative affect schedule short-form;State-trait anxiety inventory; | — |
Countries
China
Contacts
Public ContactJunhua Li
Guangzhou Medical University Affiliated Hospital of Traditional Chinese Medicine
Outcome results
None listed