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Evaluating Potential Risk of Choking by Laryngeal Ultrasound in Patients With Acute Stroke

Evaluating Potential Risk of Choking by Laryngeal Ultrasound in Patients With Acute Stroke

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04874454
Enrollment
200
Registered
2021-05-05
Start date
2023-07-14
Completion date
2026-12-31
Last updated
2025-09-19

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

Conditions

Acute Stroke

Brief summary

The investigators evaluate the vocal cord movement in patients with acute stroke by ultrasound. The occurrence of choking or aspiration pneumonia will be collected in one year after the index stroke.

Detailed description

Post-stroke dysphagia is a common complication for the stroke patient. It may cause aspiration, poor nutrition or even pneumonia; thus, it is crucial for the physicians to evaluate the swallowing function of the stroke patients. However, the evaluation methods nowadays still have some limitations. Water swallowing test is one of the well-known methods, but the test itself would put the patients at risk of aspiration. Furthermore, in order to increase the sensitivity of the water swallowing test, the amount of the water should also be increased; as a consequence, the risk of aspiration will also increase. Fiberoptic endoscopic evaluation of the swallowing and videofluoroscopy have limitations of invasiveness. The laryngeal ultrasound to evaluate the vocal cord movement can be an alternative method, having the characteristics of non-invasiveness and repeat evaluation. The investigators aim to evaluate the vocal cord movement in patients with acute stroke by ultrasound. The occurrence of choking or aspiration pneumonia will be collected in one year after the index stroke.

Interventions

DIAGNOSTIC_TESTultrasound

evaluate the vocal cord movement among the stroke patients

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* acute stroke (in one month) patients

Exclusion criteria

* patients with stroke occurring more than one month ago

Design outcomes

Primary

MeasureTime frame
the incidence of aspiration pneumoniaone year

Countries

Taiwan

Contacts

Primary ContactWan-Ching Lien
wanchinglien@ntu.edu.tw+886223123456
Backup ContactWan-Ching Lien
dtemer17@yahoo.com.tw+886988088719

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026