None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Chronic radicular pain (persistent or recurrent for > 3 months) with NRS 4 or higher - Pain that occurs or recurs after lumbar spinal surgery - After lumbar spinal surgery, the pain increases compared to before, or new radicular pain occurs that was not there before. - The site of pain coincides with the lumbar spinal surgery site dermatome. - Patients who score 4 or higher on the DN4 questionnaire and are screened for neuropathic pain - Patients whose symptoms have not improved after at least 3 months of conservative treatment - 19 = Age = 80 - Patients who voluntarily agreed in writing to participate in this clinical trial
Exclusion criteria
Exclusion criteria: - Acute phase pain less than 3 months - Patients who have not undergone lumbar spinal surgery - Radicular pain in other segments, not radicular pain consistent with lumbar spinal surgery - Axilal pain is more severe than radiating pain - Patients with adverse reactions to local anesthetics, steroids, and contrast agents - Patients with red signs such as blood clotting disorders, infections, malignant tumors, spinal fractures, progressive neurological deficits, cauda equina syndrome, etc. - Pregnant or lactating patients - If the patient does not agree to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Successful response rate | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain intensity (NRS);Oswestry Disability Index;Medication quantification scale;global perceived effect of satisfaction;Douler Neuropathique 4 | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center