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Repetitive Peripheral Magnetic Stimulation vs. Sham Procedure for Upper Limb Spasticity in Stroke Patients

Repetitive Peripheral Magnetic Stimulation vs. Sham Procedure for Upper Limb Spasticity in Stroke Patients A Double blind Randomized Controlled Trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250302001
Enrollment
32
Registered
2025-03-02
Start date
2025-04-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Stroke patients with upper limb spasticity Stroke, muscle spasticity, magnetic field therapy

Interventions

A MagRex electromagnetic stimulator device (Medical Revolution company) with a 170 mm diameter circular probe will be used. The targeted muscle groups will be the shoulder adductors and extensors, elb
Experimental Device,Sham Comparator Device
peripheral magnetic stimulation,Control

Sponsors

Faculty of medicine, Khon Kaen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Ischemic or hemorrhagic stroke diagnosed through computed tomography or MRI 2. Age between 18 to 80 years 3. Spasticity 4. Stroke duration 2 weeks to 1 year 5. No changes in anti-spasticity medications within a month before recruitment

Exclusion criteria

Exclusion criteria: 1. Use of a cardiac pacemaker or unknown invasive cardiac procedure 2. Metallic devices placed in the affected limb 3. Pregnancy 4. Malignancy 5. Botulinum toxin injection within last 6 months 6. Not follow command or cognitive impairment

Design outcomes

Primary

MeasureTime frame
Upper limb spasticity pre treatment, end of treatment and 2 weeks after treatment Modified Ashworth Scale (MAS)

Secondary

MeasureTime frame
Muscle elasticity pre treatment, end of treatment and 2 weeks after treatment Shear wave elastrography,Activities of daily living pre treatment, end of treatment and 2 weeks after treatment Barthel index,Upper limb function pre treatment, end of treatment and 2 weeks after treatment The Fugl-Meyer Assessment Upper Extremity

Countries

Thailand

Contacts

Public ContactSasithorn Khawprapa

Faculty of medicine, Khon Kaen University

info@md.kku.ac.th043348888

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026