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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04550793
Other study ID # 202006138RINB
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 2020
Est. completion date December 2021

Study information

Verified date July 2020
Source National Taiwan University Hospital
Contact Huey-Wen Liang, MD PHD
Phone 886-2-23123456
Email ntuhpmr.4124@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Spasticity of stroke patient, a very common complication in clinical practice, affects performance of hand function and gait pattern. It also interferes with quality of life of patients severely. Currently first line clinical approach to spasticity consist of physical therapy and pharmacological management. However, there are still some refractory cases that needed local intervention such as Botox injection.

So far, we only can use subjective methods to measure muscle tension, such as modified Ashworth scale and Tone Assessment Scale. In our previous study, we found that ultrasound shear wave image could correlate with muscle stiffness caused by poststroke spasticity. With this new method, we aim to establish a more objective method in measuring abnormal poststroke muscle tension before and after treatments and further monitor therapeutic effect. We also include several assessment scales to evaluate the correlation between measured muscle spasm and activity of daily living.

We hypothesize that the rheological changes in muscles muscle spasm after Botox injection can be detected by ultrasound shear wave image. Therapeutic effect can also be seen in its effect on daily functions.

In this project, we will use shear wave imaging of ultrasound to investigate the elasticity (and hardness) of the biceps brachii and brachialis muscle in stroke patients with unilateral hemiplegia before and after Botox injection. The findings of this project will provide the objective evaluation of muscle spasticity and its correlation with functional status, which will provide new points of view toward treatment of spasticity.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

[Intervention group]

- Stroke patients with unilateral involvement

- Patient's spasticity over affected upper extremities scored at least 1+ with Modified Ashworth Scale

- Patient required botulinum toxin injection at affected upper limb muscle per primary care physician.

[Control group]

- Stroke patients with unilateral involvement

- Patient's spasticity over affected upper extremities scored at least 1+ with Modified Ashworth Scale

Exclusion Criteria:

- Patients ever diagnosed with cerebral diseases other than stroke, such as traumatic brain injury, encephalitis and brain tumor

- Patients failed to cooperated due to cognition, consciousness or speech problem

- Patients with illness that could affect muscle stiffness, such as spinal cord injury and Parkinson's disease

- Patients with upper limb contracture

- Patients receiving botulinum toxin injection or shock wave therapy over upper extremities during past three months

Study Design


Intervention

Drug:
Botulinum toxin injection
Botulinum toxin injection at affected brachialis and/or biceps brachials.

Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shear Wave Ultrasound Elastography Shear wave ultrasound elastography measurement of spastic upper limb muscles, including biceps brachii and brachialis During each follow up visit within 12 weeks time frame
Secondary Barthel Index (Wade's version) Barthel Index assessing activities of daily livings During each follow up visit within 12 weeks time frame
Secondary Revised Nottingham Extended Activities of Daily Livings Scale Revised Nottingham Extended Scale assessing activities of daily livings During each follow up visit within 12 weeks time frame
Secondary Stroke Rehabilitation Assessment of Movement (STREAM), brief version STREAM assessing movement condition During each follow up visit within 12 weeks time frame
Secondary Modified Ashworth Scale (MAS) MAS scale for assessing spasticity During each follow up visit within 12 weeks time frame
Secondary Tone Assessment Scale (TAS) TAS scale for assessing spasticity During each follow up visit within 12 weeks time frame
Secondary Global improvement scale Global improvement scale for assessing symptoms related to stroke During each follow up visit within 12 weeks time frame
Secondary Self-report spasticity symptoms Self-report spasticity symptoms for assessing spasticity During each follow up visit within 12 weeks time frame
Secondary EuroQol EuroQol for evaluating quality of life During each follow up visit within 12 weeks time frame
Secondary Extended Activities of Daily Living Extended Activities of Daily Living scale for evaluating activity of daily living During each follow up visit within 12 weeks time frame
Secondary Postural Assessment Scale for Stroke Patients (PASS), brief version PASS for evaluating symptoms related to stroke During each follow up visit within 12 weeks time frame
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