None listed
Conditions
Interventions
Procedure/Surgery : Before the start of this clinical trial, all researchers participating in the trial agree on the method of treatment for the clinical trial medical device and perform the procedure
Sponsors
Seoul National University Bundang Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. 20~80 years of age at the date of written informed consent. 2. Patients who have unilateral or bilateral radiculopathy resulting from lumbar disc herniation and can be followed up for more than 1 year. 3. A person who voluntarily signed a written consent after hearing the explanation of the purpose and method of this clinical trial.
Exclusion criteria
Exclusion criteria: 1. Spondylolisthesis of Meyer Gr II or higher 2. Prior surgery at the same level 3. Lumbar degenerative scoliosis (Cobb angle>20) 4. In case of other spinal diseases in the affected area (ankylosing spondylitis, tumor, compression fracture, etc.) 5.Psychiatric illness (Dementia, mental illness) 6. Those who refused to participate in the study. 7. Others, if judged by the investigator to be inappropriate for participation in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in ODI value after 52 weeks after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| EQ-5D score changes;VAS score changes;Walking time;Satisfaction after surgery;Period to return to daily life;POSAS questionnaire;Radiological evaluation | — |
Countries
Korea, Republic of
Contacts
Public ContactSang-Min Park
Seoul National University Bundang Hospital
Outcome results
None listed