Evaluation de l'efficacité du Support Nutritionnel entéral Intermittent Sur la défaillance d'Organes de Patients de réanimation Sous Ventilation assistée ENteral NUTrition - Continue Intermittent

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to evaluate the efficiency of intermittent enteral nutrition versus continuous enteral nutrition to prevent from organ failures for patients at the acute phase of sepsis shock with mechanical ventilation in ICU.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient admitted in ICU for less than 48h, with invasive mechanical ventilation predicted for at least 48h, that can undergo nasogastric feeding for 7 days.

• Patient under vasopressive drugs

• Adult patients (age ≥ 18 years)

• Informed person who has read and signed their consent

‣ If the patient is unable to sign their consent (emergency situation), the consent will be signed by a trusted person or a family member, and consent to continue the study will be requested subsequently.

⁃ If the patient is unable to sign their consent (emergency situation) and no trusted person is present, the patient may be included in the study. In this case, consent to continue the study will be requested from a trusted person as soon as possible, or from the patient if they are able to understand and sign the consent.

• Affiliation to a social security scheme

• No current pregnancy: for women of childbearing age, a beta-HCG blood pregnancy test will be performed upon inclusion; for postmenopausal women, a confirmatory diagnosis must be obtained.

Locations
Other Locations
France
CHU de Rouen
RECRUITING
Rouen
Contact Information
Primary
Fabienne TAMION, MD
fabienne.tamion@chu-rouen.fr
+33232888261
Backup
Florian VALLIN
florian.vallin@chu-rouen.fr
+33232888265
Time Frame
Start Date: 2024-07-09
Estimated Completion Date: 2027-10-09
Participants
Target number of participants: 174
Treatments
Experimental: Intermittent enteral nutrition
patients that receive intermittent enteral nutrition.
No_intervention: continuous enteral nutrition
patients that receive continuous enteral nutrition
Related Therapeutic Areas
Sponsors
Collaborators: University Hospital, Caen, Centre Hospitalier Intercommunal Elbeuf-Louviers-Val de Reuil, Amiens University Hospital, Centre Hospitalier de Dieppe, Groupe Hospitalier du Havre, University Hospital, Lille, Centre Hospitalier Saint-Philibert, GHICL
Leads: University Hospital, Rouen

This content was sourced from clinicaltrials.gov