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Comparative study of the effects of internal heat-type acupuncture needle and transcutaneous electrical nerve stimulation on cartilage volume and clinical efficacy in patients with early to mid-stage knee osteoarthritis

Comparative study of the effects of internal heat-type acupuncture needle and transcutaneous electrical nerve stimulation on cartilage volume and clinical efficacy in patients with early to mid-stage knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080873
Enrollment
Unknown
Registered
2024-02-10
Start date
2024-02-18
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

Knee Osteoarthritis

Interventions

Experimental group:Health education and internal heat-type acupuncture needle, once a week for four weeks.
Control group:Health education once a week
transcutaneous electrical nerve stimulation three times a week for four weeks.

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for knee osteoarthritis-Guidelines for the Diagnosis and Treatment of Osteoarthritis, 2018 edition, Joint Surgery Group, Osteoscience Branch, Chinese Medical Association; 2.Kellgren-Lawrence grade?-?; 3. Between the ages of 50 and 75; 4.Pre-treatment examinations; Ensure that the patient is free of infectious diseases, related blood diseases, serious cardiovascular diseases, infections and other underlying diseases that may cause infection to the results of the study; 5. Willing to participate in the study, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.The patient is staged advanced, with a history of knee surgery (including arthroscopy, severe injury to the knee ligament, meniscus, or knee arthroplasty); 2. Other joint diseases (acute trauma, rheumatoid arthritis, septic arthritis, etc.) involving joints; 3.Those with neurological diseases (epilepsy, anxiety/depression, etc.); 4.Patients with cognitive impairment; 5.Those with MRI contraindications: equipped with metal or electronic implants, claustrophobia, etc.; 6.Patients with coagulation disorders (such as hemophilia); 7.Women who are trying to get pregnant, pregnant or breastfeeding; 8.Lidocaine allergy; 9.Patients with local sensory loss and allergy to electricity.; 10.Patients who have adverse reactions to acupuncture; 11.Those who have received acupuncture, intra-articular injection of pain relief (acetaminophen, tramadol, non-steroidal anti-inflammatory drugs, etc.) in the past 1 week, or nutritional cartilage (glucosamine, etc.); 12.Those who participate in other clinical studies during the treatment period.

Design outcomes

Primary

MeasureTime frame
Western Ontario and McMaster University Osteoarthritis Index,WOMAC;Cartilage volume;

Secondary

MeasureTime frame
Numerical rating scale (NRS);Timed Up and Go Test;36-Item Short-Form Health Survey ,SF-36;

Countries

China

Contacts

Public ContactLin Ruizhu

General Hospital of Ningxia Medical University

linruizhu05@126.com+86 135 1921 7785

Outcome results

None listed

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