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Clinical Evaluation of Sinew Dredging and Reduction Manipulation in Improving Chronic Low Back Pain of Lumbar Disc Herniation

Clinical Evaluation of Sinew Dredging and Reduction Manipulation in Improving Chronic Low Back Pain of Lumbar Disc Herniation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095426
Enrollment
Unknown
Registered
2025-01-07
Start date
2024-04-28
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Chronic low back pain of lumbar disc herniation

Interventions

Treatment group:Sinew Dredging and Reduction Manipulation combined with functional exercises
Control group:Conventional manipulation combined with functional exercises

Sponsors

Wangjing Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-65 years; (2) Meeting the diagnostic criteria for lumbar disc herniation; (3) Duration of disease >=3 months; (4) VAS pain score >=4 and<=6; (5) Those who volunteered as subjects and signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Merge with serious cardiovascular diseases (such as myocardial infarction, severe heart failure, etc.), pulmonary diseases (such as pulmonary dysfunction, etc.), kidney diseases, liver diseases, hematopoietic system diseases, etc; (2) Patients with moderate to severe osteoporosis, fractures, or other contraindications to manual manipulation; (3) Lumbar instability, lumbar spondylolisthesis, lumbar spinal stenosis, femoral head necrosis, vascular diseases, tumors, lumbar tuberculosis and other diseases, and severe neurological impairment caused by the herniation of giant nucleus pulposus; Extreme lateral protrusion causes severe radiating pain in the lower extremities; cauda equina syndrome; or have other medical conditions that require surgical treatment; (4) Used nonsteroidal anti-inflammatory and analgesic drugs or nutritional nerve drugs for treatment within 2 weeks; (5) Pregnant or lactating women; (6) Individuals who are unable to cooperate in completing the experiment due to mental illness; (7) Subjects who are currently participating in other clinical drug trials.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale/Score;

Secondary

MeasureTime frame
Oswestry disability index;Surface electromyography of the lumbar spine;

Countries

China

Contacts

Public ContactZhaojie Zhang

Wangjing Hospital of China Academy of Chinese Medical Sciences

Zhangzhaojie2010@163.com+86 136 8331 1461

Outcome results

None listed

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