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Verification of the therapeutic effect of a new physiotherapy device for synovitis associated with knee osteoarthritis:Comparison of Radial Pressure Wave(RPW)or repetitive Pulse Magnetic Stimulation(rPMS)and conventional Ultrasound therapy device(US)

Verification of the therapeutic effect of a new physiotherapy device for synovitis associated with knee osteoarthritis:Comparison of Radial Pressure Wave(RPW)or repetitive Pulse Magnetic Stimulation(rPMS)and conventional Ultrasound therapy device(US) - Verification of the therapeutic effect of a new physiotherapy device for synovitis associated with knee osteoarthritis:Comparison of Radial Pressure Wave(RPW)or repetitive Pulse Magnetic Stimulation(rPMS)and conventional Ultrasound therapy device(US)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057466
Enrollment
45
Registered
2025-04-01
Start date
2025-04-15
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

knee osteoarthritis

Interventions

radial pressure wave repetitive Pulse Magnetic Stimulation Ultrasound therapy device

Sponsors

Waseda university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who was diagnosed with knee osteoarthritis at the N Clinic and was diagnosed with intra-articular edema, and received 5 times intra-articular injections of sodium hyaluronate (HA) at a pace of once a week, and whose intra-articular effusion does not improve even after arthrocentesis is performed before sodium hyaluronate, or patients whose joint effusion or synovitis does not improve even after treatment at other clinic for more than 3 months

Exclusion criteria

Exclusion criteria: Patients who are undergoing two treatments at the same time, patients who continue to receive intra-articular HA injections, patients who have undergone focused extracorporeal shockwave therapy or other treatments (e.g., surgery, PRP therapy, APS therapy, MSC therapy, etc.) and whose therapeutic effects are thought to be involved, and patients with metabolic or infectious diseases such as RA

Design outcomes

Primary

MeasureTime frame
Investigate the amount of joint fluid punctured under the ultrasound (measure the amount of joint fluid before the start of treatment and the amount of joint fluid 5 weeks after the start of treatment) and the knee injury and osteoarthritis outcome score (KOOS) questionnaire

Secondary

MeasureTime frame
Evaluation of pain (VAS), measurement of knee joint circumference (base of the patella, mid-patella, joint fissure), evaluation of tenderness threshold (measured with an algometer),joint range of motion test (knee extension, knee flexion) measured with a goniometer,manual muscle strength test (knee extension, knee flexion) measured with a hand dynamometer Data analysis is performed using SPSS, which is a data analysis tool

Countries

Japan

Contacts

Public ContactShinya Nakasato

N clinc medical office

nakasato@n-cli.com0724-432-4976

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026