None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Adults aged 18 years or older. (2) Diagnosed with degenerative spinal disease based on radiographic and MRI findings, and requiring surgical treatment due to persistent pain despite 6 weeks of conservative management. (3) Scheduled to undergo Oblique Lumbar Interbody Fusion (OLIF) surgery. (4) Provided written informed consent to participate in this study.
Exclusion criteria
Exclusion criteria: (1) Patients under 18 years of age. (2) Patients weighing less than 45 kg or more than 100 kg. (3) Patients with severe underlying respiratory, renal, or liver disease. (4) Patients with a history of psychiatric disorders or mental illness. (5) Patients with a history of allergic reactions to local anesthetics.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compare and evaluate changes in pain relief between two groups using pain assessment tools | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate postoperative inflammatory response and possibility of infection (number of white blood cells (WBCs);Evaluation of postoperative inflammatory response and possibility of infection (Red blood cell sedimentation rate (ESR));Evaluate postoperative inflammatory response and possibility of infection (C-reactive protein (CRP)) | — |
Countries
Korea, Republic of
Contacts
Ajou University Hospital