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Comparative study on the surgical efficacy of precise and complete removal of the ligamentum flavum during endoscopic posterior approach single segment lumbar decompression surgery

Comparative study on the surgical efficacy of precise and complete removal of the ligamentum flavum during endoscopic posterior approach single segment lumbar decompression surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092321
Enrollment
Unknown
Registered
2024-11-14
Start date
2024-11-20
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Lumbar spinal stenosis

Interventions

Test Group:Accurate excision of the ligamentum flavum
Control Group:Complete excision of the ligamentum flavum

Sponsors

Xuzhou Medical University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with lumbar spinal stenosis, with symptoms of lower limb pain and intermittent claudication. 2.After 3 months of conservative treatment, it was ineffective and the symptoms affected the patient's daily life. 3. Able to follow the research protocol and follow up on schedule. 4. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Contraindications for surgery: lumbar instability, coagulation dysfunction, etc. 2. History of lumbar spine surgery in the past. 3. Narrowing of the central spinal canal beyond one segment, and it cannot be determined that the narrowing is solely caused by a single segment. 4. Simultaneously accompanied by intervertebral foramen stenosis and symptoms of intervertebral foramen stenosis. 5. LANSS score >= 12 points. 6. Other situations where posterior endoscopic decompression of the spinal canal is not suitable. 7. Other conditions (such as religion, psychology, etc.) may affect informed consent, compliance with research protocols, or inability to follow up on schedule.

Design outcomes

Primary

MeasureTime frame
ODI score one year after surgery;

Secondary

MeasureTime frame
ODI score three months after surgery;VAS scores three months and one year after surgery;Surgical time (from skin disinfection to completion of skin suturing);Postoperative hospitalization days;Postoperative analgesic medication dosage;Surgical recurrence rate;Probability of postoperative lumbar internal fixation surgery;Other postoperative complications;

Countries

China

Contacts

Public ContactLiping Chen

Pain Department of Xuzhou Medical University Affiliated Hospital

1132927346@qq.com+86 137 7587 0371

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026