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Cohort Study on the Repair of Nerve Injury in Lumbar Disc Herniation Based on Multimodal Joint Analysis of Acupuncture "deqi to the affected area" and the Neurotrophic-Inflammatory Regulatory Mechanism.

Cohort Study on the Repair of Nerve Injury in Lumbar Disc Herniation Based on Multimodal Joint Analysis of Acupuncture deqi to the affected area and the Neurotrophic-Inflammatory Regulatory Mechanism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001534
Enrollment
Unknown
Registered
2025-08-05
Start date
2025-09-01
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

deqi to the affected area:Acupuncture operation, achieving the standard of "Qi reaching the affected area" in at least 2 out of 3 treatments.
non-deqi to the affected area:Acupuncture procedure, the standard of "Qi arrival at the diseased site" was not achieved after three treatments.

Sponsors

Guangzhou University of Chinese Medicine Shenzhen Hospital(Futian)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1)Meet the diagnostic criteria for moderate radiculopathy lumbar disc herniation and the syndrome of qi stagnation and blood stasis; (2)The segment of lumbar disc herniation is between L4-S1; (3)Patients have provided informed consent and signed the informed consent form; (4)Age between 18 and 65 years old.

Exclusion criteria

Exclusion criteria: (1)Patients with free or extruded lumbar disc herniation, or cauda equina syndrome; (2)Individuals with cognitive or communication impairments, unclear consciousness, or other psychiatric disorders; (3) Contraindications to acupuncture, such as thrombocytopenia, coagulation disorders, or other significant bleeding tendencies, or skin infections/ulcers at the acupuncture site, or the presence of a cardiac pacemaker; (4) Severe cardiac, hepatic, renal, or neurological dysfunction, or uncontrolled hypertension or diabetes; (5)A history of spinal surgery or invasive lumbar examinations within the past 3 months; (6)Including lumbar spine tumors, spondylolisthesis (grade II or above), tuberculosis, bony spinal canal stenosis (sagittal diameter 30°), etc.; (7)Receipt of acupuncture, rehabilitation, massage, or related treatments, or use of medications affecting pain assessment within 1 month prior to enrollment; (8)Pregnant/lactating women, age 65 years.

Design outcomes

Primary

MeasureTime frame
The difference in Japanese Orthopaedic Association Scores scores before and after treatment.;

Secondary

MeasureTime frame
visual analogue scale;Japanese Orthopaedic Association Scores;Levels of inflammatory factors;

Countries

China

Contacts

Public ContactJianhao Huang

Guangzhou University of Chinese Medicine Shenzhen Hospital(Futian)

938396895@qq.com15880055360

Outcome results

None listed

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