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TerminatedNCT00122408Updated Sep 24, 2010

Probiotic Enteral Administration in Mechanically Ventilated Patients

A Phase 1 interventional study of Ergyphilus in Pneumonia, sponsored by Central Hospital, Nancy, France. Terminated at 3 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-09-24.

Sponsored by Central Hospital, Nancy, France · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
740
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Pneumonia

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Keywords

  • ventilator-associated pneumonia
  • probiotic
  • mechanical ventilation
  • intensive care
03

In context

Pneumonia

2,044 studies on the registry are indexed under Pneumonia; 283 are open to participants now.

This study's planned enrollment of 740 is above the median of 106 across 1,247 interventional studies indexed under Pneumonia.

Browse Pneumonia studies →

Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 778 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients under mechanical ventilation for at least 48 hours

Exclusion criteria

Exclusion Criteria:

  • Age under 18
  • Pregnancy
  • Immunocompromised status
  • Short bowel disease
  • Moribund condition
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
740 participants (estimated)

Study arms

  • Active comparator
    1

    Dietary Supplement: Ergyphilus

  • Placebo comparator
    2

    Dietary Supplement: Ergyphilus

Interventions

  • Dietary supplementErgyphilus

    5 pills a day of Ergyphilus or placebo

06

What researchers measure

Primary outcomes

  1. Intensive Care Unit (ICU) mortality rate

    Time frame: 28 days

Secondary outcomes

  1. Hospital mortality rate

    Time frame: 60 days

  2. incidence of ventilator-associated pneumonia

    Time frame: 28 days

  3. incidence of multi-resistant bacteria infection and colonization

    Time frame: 28 days

  4. incidence of diarrhea

    Time frame: 28 days

  5. ICU length of stay

    Time frame: 60 days

  6. hospital length of stay

    Time frame: 60 days

  7. antibiotic use in ICU (antibiotic-free days)

    Time frame: 28 days

07

Study locations

3 sites
  • CHG
    Macon, France
  • CHR
    Metz, France
  • Hopital Central, Service de Reanimation Medicale
    Nancy, 54000, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 24, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00122408
Lead sponsor
Central Hospital, Nancy, France
First posted
Jul 22, 2005
Start date
Jan 2006
Primary completion
Aug 2009 (estimated)
Completion
Dec 2009 (estimated)
Last update
Sep 24, 2010

Study contacts

Sebastien Gibot, MD, PhD
principal investigator · CHU Nancy
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Sep 2010. You cannot join it, but the record below documents what was studied.

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