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Probiotic Enteral Administration in Mechanically Ventilated Patients
This study is currently recruiting participants.
Verified by Central Hospital, Nancy, France, January 2006
Sponsored by: Central Hospital, Nancy, France
Information provided by: Central Hospital, Nancy, France
ClinicalTrials.gov Identifier: NCT00122408
  Purpose

The objective of this study is to assess the effects of a daily enteral supplementation with probiotics within a population of critically ill, mechanically ventilated patients. Especially, the effects of probiotics on mortality rate in intensive care medicine will be analysed.


Condition Intervention
Pneumonia
Drug: Ergyphilus

MedlinePlus related topics: Pneumonia
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Effect of Enterally Administered Probiotics in Mechanically Ventilated Patients: Double-Blind, Prospective Randomized Study Versus Placebo

Further study details as provided by Central Hospital, Nancy, France:

Primary Outcome Measures:
  • Intensive Care Unit (ICU) mortality rate

Secondary Outcome Measures:
  • Hospital mortality rate
  • incidence of ventilator-associated pneumonia
  • incidence of multi-resistant bacteria infection and colonization
  • incidence of diarrhea
  • ICU length of stay
  • hospital length of stay
  • antibiotic use in ICU (antibiotic-free days)

Estimated Enrollment: 740
Study Start Date: January 2006
Estimated Study Completion Date: December 2007
Detailed Description:

In a critically ill patient, the gut integrity is rapidly compromised either by the treatments used (such as catecholamine or antibiotics) or by the disease itself. This gut alteration favours the adhesion and/or internalisation of bacteria by intestine cells which lead to the production of large amounts of cytokines that rapidly reach the blood compartment, inducing neutrophils activation and then organ damage. Moreover, the imbalance in the normal intestinal flora (demonstrated as early as 24 hours after ICU admission) is one of the mechanisms involved in the development of ventilator associated pneumonia (VAP). VAP is the leading cause of ICU-acquired infection and is responsible for prolonged ICU stay, increased mortality and costs. Probiotics, and especially Lactobacillus Rhamnosus GG (‘LGG’), have been demonstrated to possess beneficial effects in terms of intestine flora imbalance and immune response.

Objective: To study the effects of a probiotic mixture (containing LGG) enteral administration on the survival and the incidence of VAP in mechanically ventilated patients.

Patients and Methods: Prospective, randomized, double-blind, placebo-controlled study. After randomization, 740 intubated patients with a predictive length of mechanical support of more than 48 hours will enterally receive either 10.10 cfu of probiotic (Ergyphilus, Nutergia, France) or a identical placebo daily until withdrawal of mechanical support. The main endpoint is the mortality rate in ICU. Secondary endpoints include hospital length of stay and mortality rate, VAP incidence and the number of days free from antibiotics. Length of the study 24 months.

Perspectives: The objective is to demonstrate a survival advantage due to LGG administration, along with a reduction of VAP episodes and antibiotic use.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients under mechanical ventilation for at least 48 hours

Exclusion Criteria:

  • Age under 18
  • Pregnancy
  • Immunocompromised status
  • Short bowel disease
  • Moribund condition
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00122408

Contacts
Contact: Sebastien Gibot, MD, PhD +33383852970 s.gibot@chu-nancy.fr

Locations
France
Hopital Central, Service de Reanimation Medicale Recruiting
Nancy, France, 54000
Contact: Sebastien Gibot, MD, PhD     +33383852970     s.gibot@chu-nancy.fr    
Principal Investigator: Sebastien Gibot, MD, PhD            
Sponsors and Collaborators
Central Hospital, Nancy, France
Investigators
Principal Investigator: Sebastien Gibot, MD, PhD CHU Nancy
  More Information

Study ID Numbers: promotion_070605-gibot_DRI
Study First Received: July 19, 2005
Last Updated: January 31, 2006
ClinicalTrials.gov Identifier: NCT00122408  
Health Authority: France: Afssaps - French Health Products Safety Agency

Keywords provided by Central Hospital, Nancy, France:
ventilator-associated pneumonia
probiotic
mechanical ventilation
intensive care

Study placed in the following topic categories:
Respiratory Tract Infections
Respiratory Tract Diseases
Lung Diseases
Pneumonia, Ventilator-Associated
Pneumonia

ClinicalTrials.gov processed this record on January 16, 2009