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Evaluation of the Efficiency of Intermittent Enteral Nutrition on Multi-organ Failure From Patients With Mechanical Ventilation in Intensive Care Unit

Study acronym: ENNUT-CI
StatusCompleted
PhaseNot applicable
Started2024-07-09
View on ClinicalTrials.gov ↗

Amendment history

2026-09-29
Trial completed
Primary completion confirmed: August 2026 (last estimated October 2027)
2025-06-25
Study Status, Outcome Measures v2
Secondary endpoints11 entries, revised
Evaluation of the digestive symptomstolerance
2025-06-17
Not Yet Recruiting→Recruiting Study Status, Sponsor/Collaborators, Outcome Measures, Eligibility, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2027-06-01→2027-10-09
Completion date2027-08-01→2027-10-09
Start dateestimated 2024-05-01→confirmed 2024-07-09
Study sites0→1
Eligibility criteria+896 characters
[...] icted for at least 48h, that can undergo nasogastric feeding for 7 days. Patient under vasopressive drugs PatientAdult thatpatients signed collected Patient under healthcare system Age(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 cons [...] Affiliation to a social security scheme PatientNo whocurrent haspregnancy: readfor andwomen underst [...] [...]
Secondary endpoints10 to 11 entries
Adverse events
Collaborators+240 characters
University Hospital, Lille University Hospital, Caen Amiens University Hospital Centre Hospitalier Saint-Philibert, GHICL Centre Hospitalier Intercommunal Elbeuf-Louviers-Val de Reuil Groupe Hospitalier du Havre Centre Hospitalier de Dieppe
2024-03-18
Original filing
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.
Trial Details
NCT Number NCT06330610
Lead Sponsor University Hospital, Rouen
Collaborators: University Hospital, Lille, University Hospital, Caen, Amiens University Hospital, Centre Hospitalier Saint-Philibert, GHICL, Centre Hospitalier Intercommunal Elbeuf-Louviers-Val de Reuil, Groupe Hospitalier du Havre, Centre Hospitalier de Dieppe
Conditions Intermittent Fasting, Septic Shock, Organ Failure, Multiple
Enrollment 174 participants
Start Date 2024-07-09
Primary Completion 2026-08-02 (estimated)
Study Completion 2026-08-02 (estimated)
Updated on ClinicalTrials.gov 2026-09-28