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Evaluation of Two Enteral Nutrition Strategies in Mechanically Ventilated Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00199641
First Posted: September 20, 2005
Last Update Posted: December 4, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University Hospital, Limoges
September 14, 2005
September 20, 2005
December 4, 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
Not Provided
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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
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
-Mechanically Ventilated Patients
Device: enteral nutrition
Not Provided
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
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
France
 
 
NCT00199641
DGS 2002/0361
Not Provided
Not Provided
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