Silent danger: ICU patients may choke without knowing it
NCT ID NCT07635888
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how often ICU patients silently inhale food or liquid into their lungs after a breathing tube is removed, without showing obvious signs like coughing. Researchers will compare a routine bedside swallowing test with a more detailed camera test to see if the bedside check misses these silent events. The goal is to understand risk factors and whether silent aspiration leads to worse outcomes like pneumonia or longer hospital stays.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 274 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Jun 2026
An estimate. Start dates often move.
- Expected to finish
-
Jun 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult critically ill patients admitted to the ICU who require prolonged invasive mechanical ventilation (5 days or longer) and undergo extubation. Participants will undergo bedside swallow screening and FEES evaluation after extubation to assess for silent aspiration and post-extubation dysphagia.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult ICU patients requiring invasive mechanical ventilation for 5 days or longer * Successful extubation after invasive mechanical ventilation * Undergoing bedside nursing swallow screening after extubation * Ability to undergo Fiberoptic Endoscopic Evaluation of Swallowing (FEES) within 72 hours after extubation * Provision of informed consent by the patient or legally authorized representative Exclusion Criteria: * Presence of tracheostomy * Do-not-reintubate orders/Allow natural death * Pregnancy * Absence of informed consent * Contraindication to FEES as determined by the treating physician (e.g., high bleeding risk or severe oxygen requirements)
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Critical illness are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Cleveland Clinic Abu Dhabi
Abu Dhabi, United Arab Emirates
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Why do some ICU patients bleed in the gut? researchers map the risk
- Hidden pressure: how continuous kidney dialysis may affect the abdomen in ICU patients
- Do antibiotics reach the battlefield? muscle probe tests drug delivery in sick kids
- Do ICU family meetings for the very old vary across europe?
- COVID-19's hidden toll: muscle wasting in the ICU
- Can protein and pedaling save ICU Patients' muscles?