Evaluation of Two Enteral Nutrition Strategies in Mechanically Ventilated Patients

This study has been completed.
Sponsor:
Information provided by:
University Hospital, Limoges
ClinicalTrials.gov Identifier:
NCT00199641
First received: September 14, 2005
Last updated: December 2, 2008
Last verified: December 2008

September 14, 2005
December 2, 2008
July 2002
Not Provided
Incidence of nutrition failure (diarrhea, ileus, vomiting, aspiration pneumonia, elevated residual gastric volume)
Same as current
Complete list of historical versions of study NCT00199641 on ClinicalTrials.gov Archive Site
  • -Measured nutrition amount when compared to theorical nutrition during ICU stay
  • -Measured nutrition amount when compared to theorical nutrition during the first three days
  • -Influence of prokinetic drugs on nutrition quality
Same as current
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Evaluation of Two Enteral Nutrition Strategies in Mechanically Ventilated Patients
Evaluation of Two Enteral Nutrition Strategies in Mechanically Ventilated Patients

The aim of this study is to compare two strategies of early enteral nutrition in terms of efficacy and complications in mechanically ventilated patients.

Not Provided
Interventional
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Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
-Mechanically Ventilated Patients
Device: enteral nutrition
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Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
100
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Inclusion Criteria:

  • Adult (> 18 ans)
  • Mechanical ventilation for > 72 hours
  • Planned enteral nutrition
  • Informed consent

Exclusion Criteria:

  • Body Mass Index < 20 kg/m2
  • Enteral nutrition non indicated (ileus, splanchnic ischemia..)
  • Shock (use of catecholamines, arterial blood pressure < 90 mmHg, peripheral hypoperfusion, elevation of lactates > x 1,5 normal value)
  • Contraindications for gastric tube
  • Pregnancy
  • Previous enrollment in the present study
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00199641
DGS 2002/0361
Not Provided
Not Provided
University Hospital, Limoges
Not Provided
Principal Investigator: Bruno François, MD University Hospital, Limoges
University Hospital, Limoges
December 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP