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Research on the Characteristics and Regularities of the Dose–Effect Relationship in Acupuncture

Research on the Characteristics and Regularities of the Dose–Effect Relationship in Acupuncture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002459
Enrollment
Unknown
Registered
2025-12-24
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

acute non-specific low back pain

Interventions

Deqi Acupuncture Group:Acupuncture
Sham Acupuncture (Non-Deqi) Group:sham acupuncture

Sponsors

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria Patients diagnosed with acute nonspecific low back pain (ANLBP) by a specialist physician; Onset duration =14 days, age between 18 and 65 years, with no gender limitation; Pain localized between T12 and the gluteal fold, mainly mechanical or non-radicular in nature (above the knee), originating from somatic referred pain; Pain intensity =3 on the Visual Analogue Scale (VAS); Conscious and cooperative, able to understand and complete relevant questionnaires, and willing to provide written informed consent. Note: Only patients who meet all five criteria will be eligible for inclusion in this study.

Exclusion criteria

Exclusion criteria: Exclusion Criteria Specific low back pain caused by tumor, infection, metabolic disease, rheumatoid arthritis, or fracture, or with the presence of radicular symptoms; Spinal deformities such as spondylolisthesis, spondylolysis, or scoliosis, or extramedullary diseases (e.g., vascular or genitourinary disorders); History of lumbar surgery; Low back pain accompanied by pain in more than two other body regions; Pregnant or lactating women; Patients with severe cardiovascular or cerebrovascular diseases, or with hepatic, renal, hematopoietic disorders, malignant tumors, or multiple organ failure; Patients whose emotional state fluctuates significantly or who develop psychiatric symptoms that may interfere with the study results during the research period; Patients who have received acupuncture or related treatments within two weeks prior to baseline assessment. Note: Any patient meeting any one of the above criteria will be excluded from this study.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS);

Secondary

MeasureTime frame
Oswestry Disability Index (ODI);Japanese Orthopaedic Association score for low back pain;

Countries

China

Contacts

Public ContactYu Shuguang

Chengdu University of Traditional Chinese Medicine

ysg@cdutcm.edu.cn13008165950

Outcome results

None listed

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