Evaluation of the efficacy and safety of biportal endoscopic decompressive laminectomy to treat lumbar spinal stenosis
- Conditions
- Diseases of the musculoskeletal system and connective tissue
- Registration Number
- KCT0006057
- Lead Sponsor
- Hallym University Medical Center-Kangnam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
A. 20 to 80 years old
B. Those who have a grade of B or higher for lumbar central canal stenosis and who choose to perform 1-2 segment posterior decompression
C. Those who can follow up for more than 1 year
D. Research subject who signed the consent form after fully understanding the contents of the clinical trial by the principal (if signature is possible)
A. Meyer Gr II or higher spondylolisthesis
B. Those who have previously performed the same segmental surgery
C. Lumbar degenerative scoliosis (Cobb angle> 20 degrees)
D. If the cause of the stenosis is not degenerative or due to an intervertebral disc herniation
E. If there is another spinal disease in the affected area of lumbar stenosis (ankylosing spondylitis, tumor, compression fracture, etc.)
F. Psychiatric diseases (dementia, mental retardation, severe drug addiction, etc.)
G. Those who refused to participate in the study
H. Other patients who are in charge of clinical trials as unsuitable for clinical trials
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oswestry Disability Index (ODI)
- Secondary Outcome Measures
Name Time Method Visual Analogue Scale (VAS)