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The effectiveness of treatments that targeting sinuvertebral nerve for discogenic low back pain: a prospective cohort study

The effectiveness of treatments that targeting sinuvertebral nerve for discogenic low back pain: a prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400079655
Enrollment
Unknown
Registered
2024-01-09
Start date
2022-03-23
Completion date
Unknown
Last updated
2024-01-14

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

Conservative Therapy Group:NA
Lumbar Interbody Fusion Group:NA
Intradiscal Plasma Ablation Group:NA
Sinuvertebral Nerve Injection Group:NA
Percutaneous endoscopic SVN Radiofrequency Ablation Group:NA
Percutaneous Endoscopic Lumbar Discectomy Group:NA
Percutaneous Endoscopic Lumbar Discectomy + SVN Radiofrequency Ablation Group:NA

Sponsors

Department of Spine Surgery II, The Third Affiliated Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients between 18 to 60 years old with low back pain lasting more than 6 months at the time of admission, diagnosed with the symptoms of low back pain with or without leg pain. Lumbar magnetic resonance scanning shows one or more disks degeneration (Reductive signal of the disk in T2 stage image) but without significantly herniation/protrusion (less than 50% of the spinal canal sagittal diameters), with or without high intensity zone in the posterior margin of the disk. Positive result of diagnostic lumbar sinuvertebral block is also needed but not necessary.

Exclusion criteria

Exclusion criteria: (1)History of lumbar trauma or surgery. (2)Radiological evidence of nerve root compression or excessive displacement of the vertebral body segment. (3)Facet joint degeneration (2 or more of the Weishaupt grade). (4)Paravertebral muscle degeneration (3 or more of the Goutallier grade). (5)Pathological change of the spine such as severe osteoporosis, vertebral compression fracture, tumor, or infection. (6)Vital condition is not good enough to bear the treatments. (7)Patients combine with mental illness or other cognitive impairment that affect functional evaluation. (8)Patients combine with chronic skin diseases, such ulcers, wounds, scars in the waist area.

Design outcomes

Primary

MeasureTime frame
Lumbar NRS;Lumar ODI;

Secondary

MeasureTime frame
Quality of Life;Patients' Satisfaction Degree;Return to Work/Normal Life Time;Medical Expenses;Disk Degeneration Degree;

Countries

China

Contacts

Public ContactQingchu Li

The Third Affiliated Hospital of Southern Medical University

lqc16@263.net+86 186 8022 5370

Outcome results

None listed

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