Skip to content

Clinical evaluation of high-energy shock wave therapy for knee osteoarthritis patients

Clinical evaluation of high-energy shock wave therapy for knee osteoarthritis patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082455
Enrollment
Unknown
Registered
2024-03-29
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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: Treatment was performed using a high-energy shock wave therapy device, with each treatment session lasting for 10 minutes. Three treatments were administered per week for a continu
Control group:Conventional rehabilitation treatment was administered, including exercise training and physical therapy, with each treatment session lasting for 30 minutes. Three treatments were admini

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Participants in the study were required to be between the ages of 40 and 90 2.met the diagnostic criteria for knee arthritis set by the American College of Rheumatology 3.not have undergone surgery or received special treatment 4. be able to fully participate in the study 5.have Kellgren-lawrence grades 3-4.

Exclusion criteria

Exclusion criteria: The surgical treatment of the knee, which includes arthroscopy, osteotomy, and knee arthroplasty, is contraindicated in patients with certain conditions. These conditions include the presence of thrombus in the treated area, hemorrhagic disease such as coagulopathy or hematologic disorders, severe arrhythmia, severe hypertension without blood pressure control, patients with artificial pacemaker devices, patients with multiple metastases from malignant tumors, pregnant women, patients with sensory impairment, severe rupture of tendons and fascia, patients with skin ulceration, and patients with severe cognitive impairment and psychiatric disorders.

Design outcomes

Primary

MeasureTime frame
the visual analog scale (VAS) for pain score;WOMAC score;SF-36 score; Knee Society score;patient-reported outcome measures (PROMs);infrared thermal imaging;three-dimensional gait analysis;balance function assessment; plantar pressure test;

Countries

China

Contacts

Public ContactLing REN

West China Hospital of Sichuan University

448155025@qq.com+86 159 8244 3320

Outcome results

None listed

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