Actively Recruiting
Use of Ultrasound for Early Identification of Patients at Risk of Swallowing Disorders Acquired in the ICU
Led by Centre Hospitalier Universitaire Dijon · Updated on 2026-05-12
100
Participants Needed
1
Research Sites
185 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Swallowing disorders (SD) are particularly common after extubation in the ICU and may be associated with an increased risk of lung disease, increased length of hospital stay, and a higher risk of early reintubation. In contrast, early detection of SDs has been shown to be associated with a decrease in these complications. Thus, there is a need for rapid and reliable assessment of SDs in ICU patients before the withdrawal of mechanical ventilation. Videofluoroscopy (VFS) and nasofibroscopy (NF) are the gold standard examinations for diagnosing SD. However, these two examinations are not feasible in intubated patients. In this context, ultrasound appears to be a promising alternative to identify patients at risk of SD after extubation. This examination can be performed at the intubated patient's bedside and can be used evaluate the mobility of the structures involved in swallowing. Many studies have already shown the interest of ultrasound in the evaluation of SD but none has focused on intubated patients under respiratory assistance. The objective of the present study is to evaluate the value of ultrasound in identifying patients at risk of presenting SD after extubation. This monocentric study will take place in the Intensive Care Unit (ICU) of the Dijon University Hospital. The duration of participation in this research will be equal to the length of stay in the ICU. During their stay, patients will undergo ultrasound and nasofibroscopy. Information on the characteristics of the ICU stay will be collected at discharge.
CONDITIONS
Official Title
Use of Ultrasound for Early Identification of Patients at Risk of Swallowing Disorders Acquired in the ICU
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- On mechanical ventilation for at least 48 hours
- Affiliated to national health insurance
You will not qualify if you...
- Under legal protection such as curatorship, guardianship, or safeguard of justice
- Pregnant, parturient, or breastfeeding woman
- Refusal to participate by the patient or their proxy (or an immediate family member)
- Cognitive disorders preventing understanding of instructions
- Previously diagnosed swallowing disorders
- Neurological conditions causing swallowing disorders (e.g., stroke, ALS)
- Treated for aerodigestive tract lesion by surgery, radiotherapy, or radio-chemotherapy
- Wounds or dressings preventing ultrasound measurements on the areas to be evaluated
- Decision made to limit or stop life support treatments in ICU
- Contraindications to nasofibroscopy such as nasal septum deviation or risk of significant bleeding
AI-Screening
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Trial Site Locations
Total: 1 location
1
Chu Dijon Bourgogne
Dijon, France
Actively Recruiting
Research Team
J
Jose Arturo PINEDA MASEGOSA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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