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A clinical study of endoscopic nucleus pulposus removal and annulus fibrosus suturing for treating lumbar disc herniation

A clinical study of endoscopic nucleus pulposus removal and annulus fibrosus suturing for treating lumbar disc herniation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117694
Enrollment
Unknown
Registered
2026-01-27
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Lumbar disc herniation compresses the sciatic nerve, causing radiating pain and numbness in the lower limbs

Interventions

control group:Annulus fibrosus suture
experimental group:Annulus fibrosus suture

Sponsors

Jingmen Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1.Inclusion criteria: (1) Lumbar disc herniation and lumbar spinal stenosis caused by disc herniation; 2. Preoperative symptoms of radiating pain, numbness or intermittent claudication in the lower limbs, which are ineffective after at least 6 weeks of standardized conservative treatment; 3. Based on X-ray, CT, and MRI imaging data, the diagnosis is clear and it is a single segment.

Exclusion criteria

Exclusion criteria: 1. Lumbar spondylolisthesis; 2. Lumbar spinal stenosis caused by thickening or ossification of the ligamentum flavum or space occupation in the spinal canal; 3. Recurrent lumbar disc herniation; 4. Two or more surgical segments.

Design outcomes

Primary

MeasureTime frame
The pain visual analog scale (VAS) and Oswestry Disability Index (ODI) before surgery, 3 days after surgery, and 3, 6, and 12 months after surgery were compared between the two groups to evaluate pati;

Secondary

MeasureTime frame
Recurrence rate of lumbar disc herniation;

Countries

China

Contacts

Public ContactWu Li

Jingmen Central Hospital

lw1887239@163.com+86 724 2305814

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026