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Ultrasound checks stomach fullness before tube removal in ICU

NCT ID NCT04245878

Knowledge-focused Sponsor: Centre Hospitalier Universitaire Dijon Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study involved 101 ICU patients to see if stopping their tube feeding before removing the breathing tube affects stomach fullness. Doctors used ultrasound to measure stomach content. The goal was to find ways to reduce the risk of food or liquid entering the lungs during tube removal.

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

101 people

The number who actually took part.

Started

Dec 2019

Finished

Oct 2020

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

Intensive care patients receiving respiratory assistance by mechanical ventilation

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Person or next of kin/designated representative has provided his or her non-opposition * Patient in medical or surgical intensive care, admitted for an urgent medical or surgical reason and for whom extubation have been planned by the practitioner in charge of the patient Exclusion Criteria: * Person subject to legal protection (guardianship, trusteeship) * Person subject to a justice safeguard measure * Pregnant, parturient or breastfeeding woman * Minor * Anechoic patient or patient without an exploitable ultrasound window * History of gastric or esophageal surgery * Limitation of Care (LOC) order

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Extubation Intensive care

Contacts and locations

Locations

  • Chu Dijon Bourgogne

    Dijon, 21000, France

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