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Feeding tube removal may speed up eating recovery in ICU patients

NCT ID NCT05795569

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether taking out the nasogastric feeding tube right after removing a breathing tube helps ICU patients start eating by mouth sooner. Swallowing problems are common after ICU stays, and the feeding tube itself might delay recovery. 112 adults who had been on a breathing tube for more than 48 hours took part. The main goal was to see if early tube removal shortens the time to resume eating.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

112 people

The number who actually took part.

Started

Mar 2023

Finished

Apr 2025

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.

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: * Extubation prescribed by the attending physisian * Intubation for more than 48 hours * Presence of a nasogastric tube * RASS score equal to 0 at the time of screening. Exclusion Criteria: * Gastric tube for gastric emptying (suction or bag) * Inability to remain alert for prolonged periods of time for the swallow test * Pre-existing dysphagia * Patient fed by nasogastric tube or jejunostomy before ICU stay * Tracheostomized patient * Contraindication to a bed head elevation \> 30°. * Contraindication to the resumption of feeding * Pregnant or breastfeeding woman * Decision to limit active therapies * Protected person (under guardianship or curatorship) / Person under court protection * Person not affiliated to a social security system

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Conditions

The condition(s) this trial relates to.

Deglutition Disorders eating disorder Feeding and Eating Disorders

As listed by the trial registrant

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

Contacts and locations

Locations

  • CHR d'Orléans

    Orléans, 45067, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.