Ultrasound vs. Nasofibroscopy for Evaluating Dysphagia After Extubation in the ICU
Recruiting
N/A
Interventional Study
Swallowing Disorders
Aspiration
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 40 (estimated)
- Sponsor
- Hospital H+ Queretaro · Other
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About This Trial
The goal of this observational study is to evaluate the diagnostic performance and concordance of bedside cervical ultrasonography compared to Fiberoptic Endoscopic Evaluation of Swallowing (FEES) for the early detection of post-extubation dysphagia in critically ill adult patients.
The main questions it aims to answer are:
* What is the degree of diagnostic concordance (Kappa index) between cer…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Critically ill patients admitted to the Intensive Care Unit (ICU).
* Patients aged 18 years or older.
* Patients who have required orotracheal intubation and mechanical ventilation for a period exceeding 48 hours.
* Patients successfully liberated from mechanical ventilation (…
Contacts