Herpes zoster neuralgia
Conditions
Interventions
experimental group:Medical ozone intervertebral foramen epidural injection
Control group:False injection
Sponsors
Deyang People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: 1. Men or women aged = 18 years with a history of herpes zoster = 90 days; 2. Involving spinal nerves (/thoracic/lumbar nerves); 3. The score on the Digital Rating Scale (NRS-11) is = 4 points 4. Voluntarily sign an informed consent form.
Exclusion criteria
Exclusion criteria: 1.Refusal to participate in this experiment; 2. Individuals with ozone allergies; 3. Patients with fava bean disease; 4. Pregnant or lactating women; 5. Patients with hyperthyroidism; 6. Patients with sickle cell anemia; 7. Generally, the condition is poor and cannot be treated; 8. Coagulation dysfunction, use of anticoagulants, or platelet count<70 × 10 ^ 9/l; 9. Patients with hemochromatosis or those receiving copper/iron therapy; 10. Intellectually unable to complete self-evaluation questionnaires; 11. Other situations where the researcher deems it inappropriate to enter the experiment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of postherpetic neuralgia; | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient Gender;Patient age;Hospitalization days;Ultrasound guided paraspinal nerve block treatment frequency;CT guided treatment frequency;Pain digital scores at 1 week, 2 weeks, 1 month, 2 months, 3 months, and 6 months after herpes zoster; | — |
Countries
China
Contacts
Public ContactDongmei Xiang
Deyang People's Hospital
Outcome results
None listed