Skip to content

Study on the efficacy of transcranial direct current stimulation combined with acupuncture in the treatment of osteoarthritis of the knee

Study on the efficacy of transcranial direct current stimulation combined with acupuncture in the treatment of osteoarthritis of the knee

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073819
Enrollment
Unknown
Registered
2023-07-21
Start date
2023-05-05
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

knee osteoarthritis

Interventions

Acupuncture group:acupuncture treatment
tDCS group:tDCS treatment
tDCS combined acupuncture group:tDCS combined with acupuncture treatment

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients who met the diagnostic criteria of KOA and were admitted to the hospital with a clear diagnosis and included, and patients voluntarily participated in this study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Age under 40 years; 2. Presence of metabolic-related arthritis (e.g. rheumatoid arthritis, rheumatoid arthritis, joint tuberculosis, psoriatic arthritis, etc.); 3. Recent knee trauma; 4. Presence of infectious knee disease; 5. History of previous knee surgery: e.g. knee replacement or tibial osteotomy, etc.; 6. History of knee cavity injection within the past 6 months; 7. Neurological disease: e.g. brain history of surgery, brain tumor, seizure, stroke or intracranial metal implant; 8. With severe cardiovascular disease, pulmonary disease or other serious diseases affecting survival, etc., having received other rehabilitation treatments in the last month, having used sedative drugs in the last three months, etc.; 9. Patients who did not meet the inclusion criteria and were incorrectly included; 10. Patients with incomplete final data and unable to assess the efficacy.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale (VAS);Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC);Lequesne Index;

Secondary

MeasureTime frame
Oxygenated hemoglobin (HbO2);Deoxygenated hemoglobin (HbR);Brain functional connectivity;

Countries

China

Contacts

Public ContactQiu Nie

Affiliated Hospital of North Sichuan Medical College

2022597070@qq.com+86 177 4549 5065

Outcome results

None listed

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