Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06674785

SIRS-ESWT Trial: Shoulder Internal Rotator Spasticity Trial Treated With Extracorporeal Shock Wave Therapy Trial

Led by National Taiwan University Hospital · Updated on 2025-07-29

40

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Extracorporeal shock wave therapy (ESWT) has shown potential in reducing post-stroke limb spasticity. This study aims to evaluate the efficacy of focused ESWT on shoulder internal rotator spasticity in post-stroke patients.

CONDITIONS

Official Title

SIRS-ESWT Trial: Shoulder Internal Rotator Spasticity Trial Treated With Extracorporeal Shock Wave Therapy Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older with unilateral cerebral stroke
  • Restricted passive external rotation of the spastic shoulder by more than 20 degrees
  • A Modified Ashworth Scale score of 1 or higher for shoulder internal rotator spasticity
  • Stable medical condition and vital signs
  • Clear consciousness, able to follow instructions
Not Eligible

You will not qualify if you...

  • History of two or more strokes, traumatic brain injury, brain tumors, or other cerebral disorders
  • Coexisting central nervous system disorders (e.g., spinal cord injury, Parkinson's disease) or other musculoskeletal conditions affecting muscle tone assessment
  • Ineligibility for shock wave intervention due to malignancies, coagulation disorders, localized infections, or presence of a pacemaker
  • Prior shock wave intervention or botulinum toxin injection for post-stroke spasticity within the past three months
  • Inability to participate in interventions or functional assessments due to cognitive, consciousness, or language impairments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Physical Medicine & Rehabilitation , National Taiwan University Hospital

Taipei, Taiwan

Actively Recruiting

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Research Team

S

Shu-mei Yang, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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