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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240625001
Enrollment
40
Registered
2024-06-25
Start date
2022-06-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patient who had diagnosed by clinical examination and magnetic resonance imaging identified that lumbar spinal stenosis two to three adjacent level Spinal stenosis

Interventions

alternate approach is classified that procedure was working not the same side for each level of spinal canal pathology but, they can be decompression by bilateral decompress neural element in this tec
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
Alternate approach biportal endoscopic decompression in two to three adjacent lumbar spinal stenosis ,Ipsilateral approach biportal endoscopic decompression in two to three adjacent lumbar spinal sten

Sponsors

Research Faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion 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

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

Design outcomes

Primary

MeasureTime frame
Oswestry disability index, Final modfied macnab criteria Post-op immediately, post-op 2 weeks, 4 weeks, 3 months, 6 months, 1 year Generalized estimating equation, %, disability index

Secondary

MeasureTime frame
visual analog scale, operation time, blood loss, Post op immediately, 2 weeks, 4 weeks, 3 months, 6 months, 1 year Generalized estimating equation , points , minutes, milliliters

Countries

Thailand

Contacts

Public ContactPhanurut Kaewpornmongkol

Faculty of Medicine, Srinakharinwirot University

pkaewpornmongkol@gmail.com0863560097

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026