Cervicogenic headache
Conditions
Interventions
Cervical degenerative pain control group:No cervical degenerative changes
Lumber degenerative pain control group:No lumber degenerative changes
CEH control group:Non-cervical headache
CEH group:Clinical treatment of CEH
Cervical degenerative pain group:Clinical treatment of cervical degenerative diseases
Lumber degenerative pain group:Clinical treatment of lumber degenerative diseases
Sponsors
Fifth Affiliated Hospital, Sun Yat-Sen University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Voluntarily sign informed consent; 2.Age > 18; 3.No gender limitation; 4.Guidelines for the diagnosis of cervicogenic headache in patients with a normative diagnosis of CEH; 5.Guidelines for the diagnosis of transspinal degenerative diseases in patients diagnosed with cervical degenerative changes or lumbar degenerative changes;
Exclusion criteria
Exclusion criteria: 1.Previous spinal vertebral fractures, previous spinal fusion, malformations, or symptomatic disc herniation/spinal stenosis; 2.History of spinal surgery; 3.There are some quality problems in the image, such as artifacts and deformation; 4.Pregnant women and minors are not suitable for participating in the study;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the Oswestry Disability Index scores at 3 months postoperative follow-up indicated that the pain disappeared and did not recrudesce within 3 months;the visual analogue scale at 3 months postoperative follow-up indicated that the pain disappeared and did not recrudesce within 3 months;Japanese Orthopaedic Associationscores at 3 months postoperative follow-up indicated that the pain disappeared and did not recrudesce within 3 months;Severe nausea, vomiting and even dyspnea occurred during clinical examination and treatment; | — |
Secondary
| Measure | Time frame |
|---|---|
| the Oswestry Disability Index scores at 3 months postoperative follow-up suggested pain relief within 3 months;visual analogue scale at 3 months postoperative follow-up suggested pain relief within 3 months;Japanese Orthopaedic Associationscores at 3 months postoperative follow-up suggested pain relief within 3 months; | — |
Countries
China
Contacts
Public ContactHai Lv
Fifth Affiliated Hospital, Sun Yat-Sen University
Outcome results
None listed