Lumbar Spinal Stenosis Clinical Trial
— MEDLLSSOfficial title:
Clinical Study of Microendoscopic Decompressive Laminotomy for Treatment of Lumbar Spinal Stenosis
The study is a prospective outcome study to evaluate the effectiveness and treatment
outcomes of microendoscopic decompressive laminotomy (MEDL) with objective evaluation tools.
The patients who fulfill the selection criteria will be enrolled to collect the
pre-operative clinical data including demographic data, image studies, and functional
evaluation for neurological symptoms and disability.
The patient will receive MEDL and post-operative follow-up will be arranged at 1 week, 1
month, 6 months, and 12 months after the operation. All the collected data will be analyzed
to evaluate the efficacy and treatment results of MEDL.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | December 2008 |
Est. primary completion date | December 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 40 Years and older |
Eligibility |
Inclusion Criteria: - neurogenic claudication or radicular leg pain with associated neurologic signs referring to the LSS syndrome - moderate to severe spinal canal stenosis shown on cross-sectional imaging such as MRI or CT scan - failure of conservative treatment for at least three months Exclusion Criteria: - mechanical low back pain or segmental instability |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Taiwan | Far-Eastern Memorial Hospital | Taipei |
Lead Sponsor | Collaborator |
---|---|
Far Eastern Memorial Hospital |
Taiwan,
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