Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05922085

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • On mechanical ventilation for at least 48 hours
  • Affiliated to national health insurance
Not Eligible

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

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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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