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OpenTrials
Completed

NCT Number: NCT04245878

Interest of a Period of Fasting Before Extubation in Resuscitation Patients

Orotracheal extubation in resuscitation is a situation in which there is an elevated risk of inhalation. In resuscitation, enteral nutrition that is administered in a continuous flow is likely to accumulate in the stomach. Gastric motility in resuscitation patients may be impaired for many reasons:

* Iatrogenic: Catecholamines, sedatives and opioids slow down the digestive system and decrease the tone of the lower esophageal sphincter * Shock, polytrauma, sepsis, pain or discomfort, or mechanical ventilation again create an alteration in gastric emptying.

Enteral nutrition is commonly discontinued to manage extubation, but it is not systematic. Discontinuation leads to a decrease in caloric intake.

Gastric ultrasound is a minimally invasive, reliable and promising means of monitoring that allows the stomach to be visualized directly. Studies on healthy subjects and in anaesthesia have made it possible to validate ultrasound in the context of the study of gastric content using both quantitative (including measurement of the antral area) and qualitative criteria. Measurement of the antral area was also studied in resuscitation. Antral area and gastric volume are closely related, with a correlation coefficient ranging from 0.6 to 0.91.

Identifying patients at risk of inhalation by ultrasound could allow individualized enteral nutrition management prior to extubation in the resuscitation unit, and thus optimize nutritional management.

The objective of the study is to identify factors associated with greated antral area in patients hospitalized in the intensive care unit. The hypothesis is that continued enteral nutrition before extubation is associated with increased gastric volume as measured by ultrasound.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Chu Dijon Bourgogne

Dijon, 21000, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Gastric ultrasound

Other

gastric ultrasound for measurement of the antral area

Primary outcomes

  1. Surface of the antral area in mm²

    Time frame: pre-extubation

  2. Duration of enteral feeding interruption in hours

    Time frame: pre-extubation

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire Dijon

Other

Registry information

Official study title

Interest of a Period of Fasting Before Extubation in Resuscitation Patients: a Prospective Observational Study

Acronym: NUTRIGUS

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jan 29, 2020
Registry last updated
Feb 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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