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Trial · NCT04550793

Using Shear Wave Ultrasound Elastography for Follow up After Anti-spastic Intervention Among Stroke Patients

NCT04550793, Unknown, National Taiwan University Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Using Shear Wave Ultrasound Elastography for Follow up After Anti-spastic Intervention Among Stroke Patients. Trials, record NCT04550793. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04550793

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Using Shear Wave Ultrasound Elastography for Follow up After Anti-spastic Intervention Among Stroke Patients
NCT number
NCT04550793
Status
Unknown
Enrollment
100 participants, estimated
Lead sponsor
National Taiwan University Hospital
Conditions
Stroke, Spasticity, Muscle, Botulism, Ultrasound, Activity of Daily Living
Interventions
Botulinum toxin injection
First posted
2020-09-16
Last updated
2020-09-16

Source ClinicalTrials.gov

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryShear Wave Ultrasound ElastographyDuring each follow up visit within 12 weeks time frameShear wave ultrasound elastography measurement of spastic upper limb muscles, including biceps brachii and brachialis
SecondaryBarthel Index (Wade's version)During each follow up visit within 12 weeks time frameBarthel Index assessing activities of daily livings
SecondaryRevised Nottingham Extended Activities of Daily Livings ScaleDuring each follow up visit within 12 weeks time frameRevised Nottingham Extended Scale assessing activities of daily livings
SecondaryStroke Rehabilitation Assessment of Movement (STREAM), brief versionDuring each follow up visit within 12 weeks time frameSTREAM assessing movement condition
SecondaryModified Ashworth Scale (MAS)During each follow up visit within 12 weeks time frameMAS scale for assessing spasticity
SecondaryTone Assessment Scale (TAS)During each follow up visit within 12 weeks time frameTAS scale for assessing spasticity
SecondaryGlobal improvement scaleDuring each follow up visit within 12 weeks time frameGlobal improvement scale for assessing symptoms related to stroke
SecondarySelf-report spasticity symptomsDuring each follow up visit within 12 weeks time frameSelf-report spasticity symptoms for assessing spasticity
SecondaryEuroQolDuring each follow up visit within 12 weeks time frameEuroQol for evaluating quality of life
SecondaryExtended Activities of Daily LivingDuring each follow up visit within 12 weeks time frameExtended Activities of Daily Living scale for evaluating activity of daily living

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04550793

GET https://conductscience.org/api/trials/v1/NCT04550793/registered