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Clinical Trials/TCTR20240625001
TCTR20240625001
Completed
Phase 3

Comparison clinical outcomes between Ipsilateral and Alternate-lateral Biportal endoscopic decompression for lumbar spinal stenosis

Research Faculty of Medicine0 sites40 target enrollmentJune 25, 2024

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Patient who had diagnosed by clinical examination and magnetic resonance imaging identified that lumbar spinal stenosis two to three adjacent level
Sponsor
Research Faculty of Medicine
Enrollment
40
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study suggests that both ipsilateral and alternate-lateral biportal endoscopic decompression for lumbar spinal stenosis yield similar clinical outcomes and complication rates.

Registry
who.int
Start Date
June 25, 2024
End Date
May 21, 2024
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Research Faculty of Medicine

Eligibility Criteria

Inclusion Criteria

  • 1\.Age \> 18 years old
  • 2\.Two to three adjacent levels in lumbar spinal stenosis patients
  • 3\.Low grade spondylolisthesis with lumbar spinal stenosis
  • 4\.Failed conservative for at least 3 months
  • 5\.Moderate to severe stenosis

Exclusion Criteria

  • 1\.Lumbar spinal stenosis patients who have indicated for decompression with fusion and/or instrumentation
  • 1\.1Clinical or Radiographic instability
  • 1\.2High grade spondylolisthesis
  • 1\.3Revision decompression
  • 1\.4Facet joint resection \>50%
  • 2\.Lumbar spinal stenosis patients who have causing from spinal metastasis, spinal tumor, or spinal infection
  • 3\.Double crush syndrome
  • 4\.Involuntary patients due to concern about risks of surgery, complications after surgery, financial problems, and including of subject withdrawal

Outcomes

Primary Outcomes

Not specified

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