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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1
CHG
Mâcon, France
2
CHR
Metz, France
3
Hopital Central, Service de Reanimation Medicale
Nancy, France, 54000