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Extracorporeal Shock Wave Therapy for Knee Osteoarthritis:A Randomized, Double-blind, Controlled Trial

Screening of Magnetic Resonance Pain Specific Parameters of Subchondral Bone in Knee Osteoarthritis and Study of Extracorporeal Shock Wave Therapy Strategy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069997
Enrollment
Unknown
Registered
2023-03-30
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Knee Osteoarthritis

Interventions

ESWT Group:MPT + Extracorporeal Shockwave Therapy
Sham ESWT group:MPT + sham Extracorporeal Shockwave Therapy

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: Age >= 45 years ; there was knee pain in the past 3 months ; kellgren-Lawrence ( K-L ) grade >= 2 ; signed informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: Acute knee trauma, ankylosing spondylitis, rheumatoid arthritis, psoriatic arthritis and other types of arthritis ; cardiopulmonary dysfunction, cognitive dysfunction, poor compliance and intolerance test ; intra-articular drug injection or knee surgery was performed within 6 months. There is a taboo of magnetic resonance examination ; there are contraindications for shock wave therapy such as abnormal coagulation mechanism, deep venous thrombosis of lower extremities, treatment of local peripheral tumors, infection, metal implantation, etc. Other coexisting diseases that may affect the test results.

Design outcomes

Primary

MeasureTime frame
Western Ontario and McMaster Universities Osteoarthritis Index;

Secondary

MeasureTime frame
Knee ROM;10 m walking test;Knee MRI;

Countries

China

Contacts

Public ContactLiu Xueyong

Shengjing Hospital of China Medical University

liuxy@sj-hospital.org+86 23892620

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026