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Evaluation of clinical effect of acupuncture on chronic pain of knee osteoarthritis

Evaluation of clinical effect of acupuncture on chronic pain of knee osteoarthritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078135
Enrollment
Unknown
Registered
2023-11-29
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

knee osteoarthritis

Interventions

Treatment group :Electric needle
control group:Sham acupuncture

Sponsors

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for knee osteoarthritis; 2. Aged between 50 and 75; 3. The pain lasts for more than 3 months; 4.VAS pain score 24 points; 5. Received acupuncture treatment in the last 3 months; 6. Signed informed consent, compliance is good and willing to cooperate with the research.

Exclusion criteria

Exclusion criteria: 1. Non-osteoarthritis patients with other bone diseases such as joint tuberculosis, tumor, rheumatism and rheumatoid arthritis of the knee joint; 2. Foot deformities and other lesions affecting normal walking; 3. Patients who have undergone intra-articular injection of drugs or knee arthroplasty in the past six months; 4 Patients with advanced clinical stage of knee osteoarthritis or severe articular cartilage destruction with imaging grade IV; 5. Women who are pregnant, breastfeeding or have a pregnancy plan within the last six months 6. Patients with typical cerebrovascular and nervous system diseases, or who are using drugs that have an impact on cognitive and brain function 7. There are other chronic pain patients; 8. Patients with contraindications to MRI scanning; 9. Have mental and mental disorders and can not cooperate with the questionnaire investigator; 10. Participants who are participating in other clinical trials that affect this study.

Design outcomes

Primary

MeasureTime frame
(VAS);

Secondary

MeasureTime frame
PPT;QSTs;WOMAC ;LKS;SAS;SDS;

Countries

China

Contacts

Public ContactYuan Aihong

The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine

490603279@qq.com+86 153 9500 1068

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 28, 2026