None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients aged 18 years or older Patients with available preprocedural MRI Patients clinically indicated for retrodiscal neuroplasty using a WHIP catheter due to inadequate response to conservative treatment Patients who have received sufficient explanation about the study and voluntarily provided written informed consent * Patients with available baseline clinical assessments, including NRS, ODI, medication records, and preprocedural MRI
Exclusion criteria
Exclusion criteria: Patients who do not agree to participate in the study Patients who have difficulty understanding the study procedures or are unable to communicate adequately Patients who are lost to follow-up during the study period Patients whose NRS assessment is considered to be confounded during the follow-up period due to newly developed trauma, newly diagnosed disease, conversion to surgical treatment, or other relevant events Patients whose MRI findings are not consistent with the clinical presentation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric Rating Scale (NRS);Global Improvement Score (GIS);ODI(oswestry disability index) | — |
Secondary
| Measure | Time frame |
|---|---|
| MME (morphine milligram equivalents), MQS (total medication burden);Severity of central canal stenosis;Severity of foraminal stenosis;Presence of multilevel lesions;epidurogram grade | — |
Countries
Korea, Republic of
Contacts
Seoul National University Bundang Hospital