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Clinical Trials/NCT01142570
NCT01142570
Unknown
Not Applicable

Effect of Enteral Nutrition Enriched in Protein and Based on Indirect Calorimetry Measurement in Chronically Critically Ill Patients

Rabin Medical Center0 sites60 target enrollmentSeptember 2010
ConditionsCritically Ill

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Critically Ill
Sponsor
Rabin Medical Center
Enrollment
60
Primary Endpoint
Successful weaning from ventilation
Last Updated
15 years ago

Overview

Brief Summary

This is a single-center, prospective, randomized, comparative, double-blind controlled clinical study intended to establish 1) the optimal method of determining calorie requirements and 2) the optimal amount of protein supply in chronically ventilated patients.

Detailed Description

The study will be performed in a chronic ventilation department. Enrolled patients will be randomly allocated to receive calories as dictated by: The Harriss-Benedict formula (Group 1) or Indirect Calorimetry (Group 2) After one week of admission to the hospital department and study enrollment we will review the first results of the study. After seven days of hospitalization and study enrollment patients who have not been weaned from the ventilator, will be divided into three groups. 1. Patients in the first group will receive caloric support calculated by the HARRISS BENEDICT equation and protein dose of 1.1 to 1.5 grams per kilogram weight. 2. Patients in the second group will receive caloric support as measured by indirect calorimetry and will receive protein at 1.1 grams per kilogram weight. 3. Patients in the third group will receive caloric support as measured by indirect calorimetry and will receive protein at a dose of 1.5 grams per kilogram weight. Outcome of treatment results will be performed after one ,four and eight weeks: 1. Length of hospitalization 2. Weaning from Mechanical Ventilation 3. Development and progression of pressure ulcers 4. Infectious diseases incidence 5. Amount of insulin needed for glucose control 6. Length of mechanical ventilation 7. Readmission to Intensive Care Unit 8. Mortality rate

Registry
clinicaltrials.gov
Start Date
September 2010
End Date
November 2012
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Chronically Mechanical Ventilated Patients (more than 21 days of Mechanical Ventilation) by tracheostomy,
  • Between ages 65-90

Exclusion Criteria

  • Patient over age 90 and younger the age of 65
  • PH level less than 7.3 due to metabolic causes.
  • A patient with blood albumin level less than 2.2 g / dl

Outcomes

Primary Outcomes

Successful weaning from ventilation

Time Frame: At one, four and eight weeks

Spontaneous breathing

Length of hospital stay

Time Frame: At 8 weeks

Length of hospitalization, in days

Readmission to Intensive Care Unit

Time Frame: At four and eight weeks.

Readmission to Intensive Care Unit Mortality

Time Frame: At eight weeks

Length of mechanical ventilation

Time Frame: At one, four and eight weeks

Length of mechanical ventilation in days/hours

Secondary Outcomes

  • Infectious diseases incidence(At one, four and eight weeks)
  • Development and progression of pressure ulcers(At one, four and eight weeks)
  • Checked daily insulin intake among different groups of patients(After one, four and eight weeks)

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