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Study identifier: NCT07119801 Synced from ClinicalTrials.gov · July 29, 2026
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Clinical and Ultrasonographic Evaluation of the Efficacy of Extracorporeal Shock Wave Therapy (ESWT) in Post-Stroke Spasticity

Condition: Stroke · Spastic Hemiplegia · Extracorporal Shockwave Therapy (ESWT)  ·  Sponsor: Pamukkale University

PhaseNA
Planned participants32
Who can joinAll sexes, 35 Years to 65 Years
Healthy volunteersNo

About this study

This research evaluate the effectiveness of Extracorporeal Shock Wave Therapy (ESWT) for treating spasticity in the wrist flexor muscles (flexor carpi ulnaris - FCU and flexor carpi radialis - FCR) of chronic stroke patients. Spasticity, a common complication after a stroke, causes muscle stiffness, pain, and functional limitation, leading to increased healthcare costs and a lower quality of life. Current treatments like medication and injections have significant drawbacks, such as side effects and high costs, creating a need for new, non-invasive, and effective methods. The study highlights that traditional methods for assessing spasticity, like the Modified Ashworth Scale (MAS), are subjective. It proposes using objective, non-invasive ultrasound techniques-specifically strain elastography (to measure muscle stiffness) and echogenicity (to assess muscle tissue quality)-for a more reliable evaluation. The primary goal of this research is to be the first to investigate the short- and long-term effects of ESWT on the FCR and FCU muscles using these objective ultrasound measures alongside traditional clinical scales. The findings are expected to help standardize ESWT treatment protocols and promote the use of objective ultrasound data for the management and follow-up of post-stroke spasticity.

This description comes directly from the study's public registry record.

Talk to the study team

Meltem Güneş Akıncı, Assistant professor  ·  +905375145590  ·  meltem_aytekin@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Pamukkale UniversityDenizli, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07119801