Skip to content

Use of Ultrasound for Early Identification of Patients at Risk of Swallowing Disorders Acquired in the ICU

Use of Ultrasound for Early Identification of Patients at Risk of Swallowing Disorders Acquired in the ICU

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05922085
Acronym
EIDAR
Enrollment
100
Registered
2023-06-28
Start date
2023-11-09
Completion date
2027-06-01
Last updated
2026-05-12

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

Conditions

Patient Under Mechanical Ventilation

Brief summary

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.

Interventions

OTHERUltrasound

performed within 3 hours prior to extubation

OTHERnasofibroscopie

performed within 3 to 24 hours after extubation

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

Patient: * Major (≥18) * On mechanical ventilation for at least 48 hours * Affiliated to national health insurance

Exclusion criteria

Patient: * Under legal protection (curatorship, guardianship, safeguard of justice) * Pregnant, parturient or breastfeeding woman * Refusal to participate by the patient or their proxy (or an immediate family member) * Cognitive disorders incompatible with the understanding of instructions * Previously diagnosed swallowing disorders * With a neurological condition at the origin of the SD (stroke, ALS...) * Treated for a lesion of the aerodigestive tract (by surgery, radiotherapy or radio-chemotherapy) * presence of wounds or dressings on the areas to be evaluated that prevent ultrasound measurements * Patient for whom a decision to limit or stop life support treatments has been taken collegially within the intensive care unit * With one or more contraindications to performing NF: * Anatomical features not compatible with NF: mainly deviation of the nasal septum. * Risk of significant otorhinolaryngological bleeding

Design outcomes

Primary

MeasureTime frameDescription
rate of swallowing disordersWithin 3 to 24 hours of extubationassessed by the Penetration-Aspiration Scale (PAS)

Secondary

MeasureTime frameDescription
Presence (PAS score >2 for at least one of the food textures) or absence of SD evaluated by FEESwithin 3 to 24 hours following extubation
Presence (PAS score > 2 for thick liquids) or absence of severe SD, evaluated by FEESWithin 3 to 24 hours following extubation
Relationship between the presence or absence of SD and global muscle strengthWithin 3 hours prior to extubationAssessed by the MRC scale measurement before extubation
Relationship between the presence or absence of SD and muscle mass evaluated by ultrasoundWithin 3 hours prior to extubationThickness of the right QF and cross-sectional area of the right RF muscle at rest
Relationship between the presence or absence of SD and cough strength before extubationBefore extubationEvaluated by measuring the Peak Expiratory Flow (PEF) on the ventilator
Concordance between the assessement of parameters measured during the FEES procedure by the otolaryngologistWithin 3 to 24 hours following extubationKappa for qualitative variables
Feasibility of the ultrasound examinationWithin 3 hours prior to extubationProportion of ultrasounds performed (number of ultrasounds performed / number of eligible extubated patients) Identification of the reasons for not performing the ultrasound (e.g., physiotherapist unavailability, patient refusal) Proportion of uninterpretable ultrasounds (number of uninterpretable ultrasounds/number of ultrasounds performed) Identification of the reasons for uninterpretability of the ultrasound Mean time taken to perform the ultrasonographic assessment
Presence (PAS score > 2 for water) or absence of mild SD, evaluated by FEESWithin 3 to 24 hours following extubation
Concordance between the assessement of parameters measured during the FEES procedure by the intensivistWithin 3 to 24 hours following extubationkappa for qualitative variables

Countries

France

Contacts

CONTACTJose Arturo PINEDA MASEGOSA
josearturo.pinedamasegosa@chu-dijon.fr03 80 29 37 51

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026