Status:

TERMINATED

Probiotic Enteral Administration in Mechanically Ventilated Patients

Lead Sponsor:

Central Hospital, Nancy, France

Conditions:

Pneumonia

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief 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...

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 adh...

Eligibility Criteria

Inclusion

  • Patients under mechanical ventilation for at least 48 hours

Exclusion

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

Key Trial Info

Start Date :

January 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2009

Estimated Enrollment :

740 Patients enrolled

Trial Details

Trial ID

NCT00122408

Start Date

January 1 2006

End Date

December 1 2009

Last Update

September 24 2010

Active Locations (3)

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Page 1 of 1 (3 locations)

1

CHG

Mâcon, France

2

CHR

Metz, France

3

Hopital Central, Service de Reanimation Medicale

Nancy, France, 54000

Probiotic Enteral Administration in Mechanically Ventilated Patients | DecenTrialz