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Pulsed Electromagnetic Fields for the Management of Knee Osteoarthritis: A Multicenter, Randomized, Controlled, Non-inferiority Trial

Pulsed Electromagnetic Fields for the Management of Pain, Function, and Activities Among People with Knee Osteoarthritis: A Multicenter, Randomized, Controlled, Open-label Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052131
Enrollment
Unknown
Registered
2021-10-19
Start date
2021-10-31
Completion date
Unknown
Last updated
2022-06-27

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:PEMFs+sham drug
Control group:celecoxib+sham PEMFs

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=40 years old; 2. Patients diagnosed with knee arthritis (according to the "Guidelines for the Diagnosis and Treatment of Osteoarthritis (2018 Edition)" by the Orthopaedic Branch of the Chinese Medical Association and the diagnostic criteria for knee osteoarthritis formulated by the American College of Rheumatology in 2012; 3. Kellgren-Lawrence grading of knee joint 2-3; 4. NRS pain numerical score 4-6 points; 5. No obvious deformity; 6. Not participating in other clinical trials; 7. Can walk independently; 8. No recent surgery is considered; 9. Understand and sign the content of the informed consent form.

Exclusion criteria

Exclusion criteria: 1. No other joint diseases; 2. Knee replacement surgery or intracavitary injection therapy (within 6 months); 3. Diagnosed with rheumatoid arthritis or suspected other pathological conditions of the knee joint; 4. Previous use of PEMFs; 5. Unstable condition, suffering from mental illness such as depression and anxiety; 6. Have taken NSAIDs, opioids, amino acid glucose or other analgesics one week before enrollment; 7. Patients with intolerance to analgesics such as acetaminophen and NSAIDs.

Design outcomes

Primary

MeasureTime frame
The Western Ontarioand McMaster Universities for pain and physical function;

Secondary

MeasureTime frame
digital pain score;Quality of life score;The Western Ontarioand McMaster Universities for stiffness;6 Mimute-Walking Test;

Countries

China

Contacts

Public ContactHe Chengqi

West China Hospital of Sichuan University

hxkfhcq2015@126.com+86 18980601618

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026