Ultrafast Ultrasonographic Oro-laryngeal Measurement in Critically Ill Patients During Weaning From Mechanical Ventilation
NCT ID: NCT05611437
Last Updated: 2023-02-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
150 participants
OBSERVATIONAL
2022-12-01
2024-08-31
Brief Summary
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Post-extubation stridor is a clinical sign of upper airway obstruction and may require urgent reintubation, which is associated with increased patient length of stay, morbidity and mortality.
Identifying patients at risk is critical, and the need for reliable tools to predict the occurence of laryngeal edema is still relevant.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Ultrafast ultrasonography
Ultrasonography of the neck, patient in supine position, neck hyper-extended. Three different scanning planes containing several landmarks. Carried out in the 12h prior extubation.
Eligibility Criteria
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Inclusion Criteria
* Intubated and ventilated for more than 24h,
* Filing mechanical ventilation weaning criteria.
Exclusion Criteria
* Under guardianship patient,
* History of laryngeal tumor, stroke, paralysis of recurrent nerve, swallowing disorders,
* History of surgical laryngeal intervention or radiotherapy,
* Unplanned extubation,
* Opposition to take part in the study.
18 Years
ALL
No
Sponsors
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Groupe Hospitalier du Havre
OTHER
Responsible Party
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Locations
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Groupe Hospitalier du Havre
Montivilliers, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2022-A01363-40
Identifier Type: -
Identifier Source: org_study_id
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