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Measurement of Intestinal Permeability in Intensive Care Patients With Single or Multiple Organ Failure

Measurement of Intestinal Permeability in Intensive Care Patients With Single or Multiple Organ Failure

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06845865
Acronym
BLUE-REA
Enrollment
126
Registered
2025-02-25
Start date
2025-02-20
Completion date
2029-04-30
Last updated
2026-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infection in ICU, Monovisceral Failure, Multivisceral Failure Syndrome

Brief summary

Multivisceral failure syndrome (MVFS) in humans is associated with a very high risk of mortality, ranging between 30 and 50%. This syndrome is associated with significant systemic inflammation and a high risk of bacteremia, the origin of which is not always identified. Among the possible causes of bacteremia, digestive translocation is the most probable but has not been formally proven to date. This translocation is made possible by the numerous cellular and metabolic alterations secondary to MVFS, which can lead to increased intestinal barrier permeability. Intestinal permeability is currently not systematically evaluated in clinical practice in humans. This increased intestinal permeability, associated with the presence of inflammatory markers and a septic state, has been studied in several animal models ranging from the fruit fly (Drosophila) to the mouse. These studies have shown a high risk of mortality associated with increased intestinal permeability. We propose to use this methodology in intensive care patients with at least one organ failure to investigate the link between increased intestinal permeability and survival chances.

Interventions

DIETARY_SUPPLEMENTenteric dyed solution

Oral administration of 0.5 mg/kg of body weight of food coloring dye

Sponsors

Direction Centrale du Service de Santé des Armées
Lead SponsorOTHER
Centre Borelli UMR 9010
CollaboratorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patient with single organ failure, secondary to sepsis, hospitalized in intensive care for a foreseeable duration of \> 48 hours * SAPS2 between 20 and 40 at the sixth hour after the diagnosis of organ failure. * Consent from the patient or their trusted person. * Affiliation to a social security system. * Functional digestive tract and possible feeding (per os or via a nasogastric tube whose indication was determined independently of the study's needs). Second group of patients with multi-organ failure: * Multi-organ failure syndrome with at least 2 organ failures, secondary to sepsis. * SAPS2 between 60 and 80 at the sixth hour after the diagnosis of organ failure. * Consent from the patient or their trusted person. * Affiliation to a social security system. * Functional digestive tract and possible feeding (conscious patient able to swallow or with a nasogastric tube whose indication was determined independently of the study's needs).

Exclusion criteria

* Pregnant and breastfeeding women; * Minors; * Persons under administrative and judicial supervision; * Absence of a functional digestive tract (patient unable to swallow and absence of a nasogastric tube, contraindication to enteral feeding); * Patients with gastroparesis; * Refusal of the patient or their trusted person; * Patient with a SAPS2 at the sixth hour after the diagnosis of organ failure \< 20 or between 40 and 60 or \> 80.

Design outcomes

Primary

MeasureTime frameDescription
intestinal failure and survival 90 days post inclusion2024-2027Evaluation of the impact of changes in permeability (classified into 3 categories: absent, moderately increased, and highly increased) on patient survival at day 90

Secondary

MeasureTime frameDescription
intestinal permeability as a function of organ failure2024-2027Comparison of average intestinal permeability between patients with a single organ failure versus multiple organ failures on day 1 in the blood (plasma)

Countries

France

Contacts

CONTACTMichael RERA, PhD
michael.rera@cnrs.fr+33781945974
CONTACTRachel HAUS, PhD
evdg-dpar.contact.fct@intradef.gouv.fr
PRINCIPAL_INVESTIGATORClément DUBOST, MD, PhD

National teaching army hospital BEGIN (Hôpital National d'Instruction des Armées BEGIN)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 1, 2026