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Comparison of outcomes of whether incising annulus fibrosus and removing nucleus pulposus via percutaneous endoscopic spinal surgery for lumbar spinal stenosis combined with contained lumbar disc herniation

Comparison of outcomes of whether incising annulus fibrosus and removing nucleus pulposus via percutaneous endoscopic spinal surgery for lumbar spinal stenosis combined with contained lumbar disc herniation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020228
Enrollment
Unknown
Registered
2018-12-20
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Lumbar spinal stenosis

Interventions

treatment group:incise annulus fibrosus and remove nucleus pulposus
control group:not incise annulus fibrousus

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) manifested as unilateral single-level radicular symptoms: buttock or leg pain, numb,or weakness, with or without low back pain; (2) radiological diagnosis of lumbar spinal stenosis combined with contained lumbar disc herniation, and the radiological diagnosis should be identical to clinical findings; (3) dissatisfication for conservative treatment for more than 3 months; (4) accept the operation and agree to accomplish all follow-up.

Exclusion criteria

Exclusion criteria: (1) combined with noncontained herniation; (2) combined with lumbar segemental instability or spondylolisthesis (more than I degree); (3) previous history of spinal surgery for the target level; (4) combined with tumor, infection, fracture, etc; (5) intolerance of operation.

Design outcomes

Primary

MeasureTime frame
VAS of pain;ODI index;MacNab criteria;satisfactory rate;complication;

Countries

China

Contacts

Public ContactQingquan Kong

West China Hospital, Sichuan University

kongspine@126.com+86 15982835131

Outcome results

None listed

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