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Observational study on the immediate efficacy of auricular acupuncture combined with active exercise in the treatment of acute lumbar sprain

Observational study on the immediate efficacy of auricular acupuncture combined with active exercise in the treatment of acute lumbar sprain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083740
Enrollment
Unknown
Registered
2024-04-30
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Acute lumbar sprain

Interventions

Sponsors

Second Affiliated Hospital of Yunnan University/ School of Acupuncture and Massage-Rehabilitation/ The Second AfiliatedHospital, Yunnan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for ALS; (2) unilateral low back pain, age 18-60 years; (3) duration of the disease = 3 days; (4) moderate to severe low back pain, with a Visual Analogue Score (VAS) between 4 and 8; (5) signed the informed consent form. (Note: Patients who meet the above 5 items at the same time may beincluded in this study)

Exclusion criteria

Exclusion criteria: (1) Combination of lumbar spondylolisthesis, lumbar spine tumour, fracture and other diagnosed definite pathological changes of the lumbar spine; (2) Low back pain caused by internal medicine diseases; (3) Coexistence of cardiovascular, hepatic, renal, pulmonary and haematopoietic systems and other serious primary diseases; (4) Severe mental illness or intellectual disability, unable to cooperate with the completion of the questionnaire; (5) Women in pregnancy or breastfeeding; (6) Fear of acupuncture , or contraindication to needling such as skin infection or breakage at the acupoint site; (7) Other analgesic methods used in the past 6 hours.(Note: Patients meeting any of the above criteria wil be excluded)

Design outcomes

Primary

MeasureTime frame
Pain intensity at 10 minutes;

Secondary

MeasureTime frame
Pain intensity at other times;Lumbar spine mobility score;Blinded evaluation;Efficacy expectation scale evaluation;

Countries

China

Contacts

Public ContactGuo Taipin

Yunnan University of Chinese Medicine

gtphncs@126.com+86 184 8727 2658

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026