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Clinical Study on the Treatment of Knee Osteoarthritis by Acupuncture of Spirit-regulating Method

Clinical Study on the Treatment of Knee Osteoarthritis by Acupuncture of Spirit-regulating Method

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080288
Enrollment
Unknown
Registered
2024-01-25
Start date
2024-01-31
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

knee osteoarthritis

Interventions

control group:Local Acupuncture for the Knee Joint
experimental group:Local Acupuncture for the Knee Joint + Tousanshen Acupoint

Sponsors

Dongfang Hospital Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Meet the western medical diagnostic criteria for knee osteoarthritis; ? Unilateral/bilateral knee pain with a disease duration of more than half a year; ? Patients aged 40 to 75 years; ? Radiological examination within 6 months shows KL grading ?-?; ? NRS score =4 in the past week; ? All patients volunteered to participate in this clinical study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: ?Those who have serious abnormal reaction to acupuncture stimulation (e.g., fainting from needles, allergy to needles, etc.) and cannot adhere to acupuncture; ? Patients who have been taking long-term medications such as non-steroidal anti-inflammatory drugs (NSAIDs), glucocorticosteroids, or painkillers that may affect the efficacy of the treatment; ? Those who have a history of knee surgery or are waiting for knee surgery (knee replacement or knee arthroscopy); ? Knee pain caused by other diseases (e.g. joint free body, serious fluid accumulation in the joint cavity, infection, malignant tumour, autoimmune disease, trauma, fracture, gout, lumbosacral spine disease, etc.); ? Serious cardiac, hepatic, renal and coagulation abnormalities; ? Pregnant and breastfeeding women; ? Combined mental illnesses who cannot cooperate with the treatment.

Design outcomes

Primary

MeasureTime frame
Numerical Rating Scale;Western Ontario and MCMaster Universities Osteoarthritis Index;

Secondary

MeasureTime frame
Self-Rating Anxiety Scale;3-level version of Euro Qol five-dimension questionnaire;Disappearance rate of major symptoms;

Countries

China

Contacts

Public ContactYuan Li;Hua Li

Dongfang Hospital Beijing University of Chinese Medicine

lihua19831983@sina.com+86 178 0121 9951

Outcome results

None listed

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