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Clinical efficacy and safety analysis of two minimally invasive endoscopic techniques and traditional surgery for lumbar spinal stenosis

Clinical efficacy and safety analysis of two minimally invasive endoscopic techniques and traditional surgery for lumbar spinal stenosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077488
Enrollment
Unknown
Registered
2023-11-10
Start date
2023-11-11
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

lumber spinal stenosis

Interventions

Sponsors

Weifang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Single-stage lumbar spinal stenosis; (2) Typical neurogenic intermittent claudication with bilateral limb neurological damage, and no significant improvement after 3 months of conservative treatment; (3) Aged 40-80 years old; ( 4) Sign the informed consent form and be able to accurately read or understand the informed consent form and follow-up related questionnaires when accompanied by family members; (5) Be able to agree to and fully comply with the clinical plan and be willing to comply with the follow-up schedule and requirements.

Exclusion criteria

Exclusion criteria: (1) Spinal stenosis caused by fractures, tumors and infections; (2) History of spinal surgery; (3) Complete paralysis of the limbs; (4) Contraindications to surgery or refusal of surgical treatment; (5) Suffering from mental and psychological disorders, such as Schizophrenia, depression, history of taking chronic analgesics, alcoholism, and opioid dependence; (6) Other conditions that the researcher deems inappropriate for this study.

Design outcomes

Primary

MeasureTime frame
Oswestry Dability index, ODI;Japanese Orthopedic Association ,JOA;visual analogue scale score after operation;Intraoperative bleeding volume;

Secondary

MeasureTime frame
Increase rate of cross-sectional area of dural sac after operation;Preoperative dural sac area;Postoperative hospital stay;Perioperative complications;

Countries

China

Contacts

Public ContactBingwu Wang

Weifang People's Hospital

bwwspine@126.com+86 156 8922 6708

Outcome results

None listed

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