None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Adults aged 19 years and over, but not older than 89 years (2) Patients clinically diagnosed with degenerative lumbar disorders (herniated disc, spinal stenosis, or spondylolisthesis) who require 1-2 level posterior lumbar fusion (3) Patients willing to participate in the study, adhere to treatment and procedures, and attend all follow-up evaluations (4) Patients who have voluntarily signed a written informed consent form after receiving an explanation of the study's purpose, methods, and potential effects
Exclusion criteria
Exclusion criteria: (1) Patients under 18 years old or over 90 years old (2) Patients unable to undergo spinal surgery under general anesthesia due to severe cardiac, pulmonary, hepatic, or renal conditions (3) Patients undergoing surgery for intradural tumors (4) Patients on long-term steroid therapy (5) Patients diagnosed with osteoporosis prior to surgery or with preoperative screening results showing BMD = -2.5 (6) Obese patients with a BMI > 35 kg/m²
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of patients' quality of life using the 36-Item Short Form Survey (SF-36) | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of patients' pain levels using the Visual Analogue Scale (VAS);Assessment of lumbar functional disability using the Oswestry Disability Index (ODI);Bone fusion rate: evaluated using postoperative imaging studies (X-ray, CT scan);Alignment and subsidence: evaluated using postoperative imaging studies (X-ray, CT scan) | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center