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Efficacy of percutaneous transforaminal endoscopic discectomy resection of sinus nerves in the treatment of discogenic low back pain

Efficacy of percutaneous transforaminal endoscopic discectomy resection of sinus nerves in the treatment of discogenic low back pain

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026758
Enrollment
Unknown
Registered
2019-10-20
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-10-21

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

Conditions

discogenic low back pain

Interventions

Experimental group:Endoscopic resection of sinus nerves

Sponsors

The Third Affiliated Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Chronic low back pain is accompanied by more than two clinical manifestations: sedentary pain, back stretching pain, and difficulty in relieving or maintaining the same posture; 2. Skeletally mature patients with chronic (>=6 months) isolated lumbar back pain, who had not responded to at least 6 months of nonoperative management; 3. MRI evidence of intervertebral disc degeneration.with or without annular tear; 4. Complete medical record; 5. Volunteer to participate in the trial, and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Previous lumbar spine surgery; 2. Symptomatic spinal stenosis; 3. Metabolic bone disease, spine fragility fracture history, or trauma/compression fracture,or spinal cancerSpine infection, active systemic infection, bleeding diathesis; 4. Cardiovascular diseases such as cardiovascular and digestive system and other serious diseases; 5. Pregnant and lactating women; 6. Liver and kidney dysfunction; 7. Other autoimmune diseases, allergic diseases and acute and chronic infections; 8. Chronic skin disease or operation area with skin ulcer wound scar; 9. The researchers did not think it would be appropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
VAS scoring (visual analogue scoring system);

Countries

China

Contacts

Public ContactQingchu Li

Department of Orthopedics, The Third Affiliated Hospital of Southern Medical University

liqingchu12@qq.com+86 18680225370

Outcome results

None listed

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