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Clinical Study on Digital Electric Fire Needle Treatment for Lumbar Disc Herniation

Clinical Study on Digital Electric Fire Needle Treatment for Lumbar Disc Herniation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106764
Enrollment
Unknown
Registered
2025-07-30
Start date
2025-07-31
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Lumbar disc herniation

Interventions

Treatment group (digital electric fire needle group):Digital electric fire needle Therapy
Control group (Pseudo-fire Needle group):Pseudo-fire Needle Therapy

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18~65 years old; Male or female is not limited; 2. Meet the diagnostic criteria of lumbar disc herniation in traditional Chinese and Western medicine, and the protrusion site is L4/5~L5/S1; 3. Occur with at least one symptom of lumbar disc herniation: low back pain or hip pain; pain and/or numbness in the lower extremities; radiating pain in the lower extremities; 4. Visual Analogue Scale (VAS) score >=4 points; 5. Body mass index (BMI) between 18.5~24 kg/m^2; 6. Volunteer to participate in this trial, understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who have lumbar spinal stenosis, lumbar spondylolisthesis, lumbar infectious diseases, and lumbar spine tumors; 2. Lumbar spine fracture, severe osteoporosis, bone destruction caused by bone tumors, etc. with similar symptoms to LDH. 3. Meet the surgical indications for lumbar disc herniation emergencies, such as fecal incontinence and saddle paresthesia caused by compression of the cauda equina nerve, paralysis of the muscles of the lower extremities or sensory disturbances caused by single nerve paralysis, etc.; 4. Those with severe mental illness and cognitive dysfunction; 5. Patients with diabetes mellitus with poor blood sugar control, cardiovascular and cerebrovascular, liver, kidney and hematopoietic system, and patients with acute infectious diseases; 6. Those who have ulcers, unexplained lumps and bleeding on the skin at the waist acupuncture points are not suitable for acupuncture intervention; or abnormal coagulation function; 7. Pregnant or lactating women; 8. Participating in other clinical trial investigators;

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;

Secondary

MeasureTime frame
JOA Low Back Pain Score;Modified Oswestry Disability Index;IL-6;TNF-a;CXCL12;

Countries

China

Contacts

Public ContactWang Shuxin

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

widiot@126.com+86 136 6028 5076

Outcome results

None listed

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