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The Clinical Evaluation of Lumbar Spinal Stenosis with Stand-Alone Oblique Lateral Interbody Fusion: a Retrospective Study Based on Medical Records

Efficacy of Indirect Decompression in Lumbar Spinal Stenosis with Stand-Alone Oblique Lateral Interbody Fusion: a Retrospective Study Based on Medical Records

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052419
Enrollment
Unknown
Registered
2021-10-25
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Lumbar Spinal Stenosis

Interventions

case series:Nil

Sponsors

Yijishan Hospital of Wannan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were diagnosed as lumbar spinal stenosis with grade A-C according to Schiass study ; 2. Segments of lumbar spinal stenosis were located from L2 to L5; 3. Patients who experienced chronic low back pain and radiating pain to the lower extremities and could not be effectively treated conservatively for at least 3 months.

Exclusion criteria

Exclusion criteria: 1. The facet joint was fused spontaneously according to the CT scan; 2. Patients with severe osteoporosis (the T value of bone density was less than -2.5); 3. Patients who were diagnosed with traumatic injuries, tumors, or infections of lumbar.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale;Oswestry disability index;Disc height;Foraminal height;Lumbar lordosis;—

Countries

China

Contacts

Public ContactXu Hongguang

Yijishan Hospital of Wannan Medical College

xuhgyjsyy@163.com+86 13855386303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026