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Ultrasound guided myofascial pulsed radiofrequency or combined with sodium hyaluronate in the treatment of knee osteoarthritis

Ultrasound guided myofascial pulsed radiofrequency or combined with sodium hyaluronate in the treatment of knee osteoarthritis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045357
Enrollment
Unknown
Registered
2021-04-13
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-11-22

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

Conditions

Knee osteoarthritis

Interventions

Pulsed radiofrequency group:Trigger point pulsed radiofrequency
Sodium Hyaluronate Group:Sodium Hyaluronate Injection into Knee Joint Cavity
Joint Intervention Group:Trigger point pulsed radiofrequency and Sodium Hyaluronate Injection into Knee Joint Cavity

Sponsors

The First Affiliated Hospital of Suzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria for knee osteoarthritis in the "Guidelines for the Diagnosis and Treatment of Osteoarthritis"; 2. Have not received invasive treatment for the knee joint in the past month; 3. Volunteer to participate in this experimental study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe knee deformities; 2. Severe ankle and hip joint disease; 3. Patients with significant narrowing of knee arthritis gap or bone ankylosis connected by arthritic bone bridge; 4. Patients with local skin ulcers or intra-articular infections in the knee joint; 5. Patients with rheumatoid diseases; 6. Patients with a history of convulsions; 7. Women during pregnancy and lactation; 8. Patients with malignant tumors or patients with severe osteoporosis caused by long-term high-dose use of hormones; 9. Diseases that seriously affect the joints, such as knee joint tumors, rheumatoid arthritis, tuberculosis, suppuration, etc.

Design outcomes

Primary

MeasureTime frame
WOMAC Score Scale;Visual Analogue Score;

Secondary

MeasureTime frame
Knee joint range of motion;Trigger Point Tenderness Threshold Measurement;

Countries

China

Contacts

Public ContactWang Lina

The First Affiliated Hospital of Suzhou University

wangln@suda.edu.cn+86 13915400622

Outcome results

None listed

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