Phase
Condition
N/ATreatment
enteric dyed solution
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
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 tubewhose 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 swallowor with a nasogastric tube whose indication was determined independently of thestudy's needs).
Exclusion
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 anasogastric 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 orbetween 40 and 60 or > 80.
Study Design
Connect with a study center
Hopital Bégin
Vincennes,
FranceActive - Recruiting
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