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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00256074
Other study ID # 2003.263
Secondary ID
Status Terminated
Phase N/A
First received November 17, 2005
Last updated April 10, 2017
Start date June 2004
Est. completion date November 2007

Study information

Verified date April 2017
Source Melbourne Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the impact of different feeding solutions on patients with breathing difficulty being supported by a breathing machine.

The aim of the study is to determine if high fat-low carbohydrate feeding reduces the carbon dioxide production in patients with respiratory failure.


Description:

Patients who agree to participate in the study and fulfil the inclusion criteria, will be randomised to one of two treatment groups.

1. Standard therapy group. Will receive high carbohydrate, low fat enteral feeding, (16.7% protein, 30% fat and 53.3% carbohydrate). The target rate is determined by the treating physician and dietician, for a minimum of 5 days following randomisation.

2. Alternative therapy group will receive high-fat, low carbohydrate enteral feeding, (16.7% protein, 55.2% fat and 28.1% carbohydrates. At a target rate determined by the treating physician and dietician, for a maximum of 5 days following randomisation.

All patients will receive enteral feeding by continuous flow for 24 hours a day. The decision to commence or cease enteral feeding will remain with the treating physician.

The measurement of VO2, VCO2, resting energy expenditure and respiratory quotient wil be made on all participants 12 hourly for a maximum of 5 days using the direct calorimeter. The indirect calorimeter is connected to the expiratory outlet of the ventilator, collecting and analyzing gas that is normally discharged in to the atmosphere.

The hypothesis of the study is that the use of high- fat, low-carbohydrate enteral feed, significantly reduces the carbon dioxide production and the respiratory quotient in critically ill, mechanically ventilated patients with respiratory failure. Compared to standard high-carbohydrate low-fat enteral feed.


Recruitment information / eligibility

Status Terminated
Enrollment 30
Est. completion date November 2007
Est. primary completion date November 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Adult patient, 18 years or older admitted with acute respiratory failure (PaO2/FiO2 <300), needing mechanical ventilation. Are expected to be require mechanical ventilation for more than 48 hours.

2. Patients who are to receive enteral feeding via a gastric or post-pyloric feeding tube.

3. Patients or their next-of-kin consent to participate in the study. -

Exclusion Criteria:

1. Patients under the age of 18 years

2. Patients with contra-indications to enteral feeding

3. Patients receiving total parental nutrition

4. Patients who are already enrolled in another study that may influence the outcome of this study.

5. Patients who are not receiving active medical management or are expected to die within 24 hours at the time of study entry.

6. Patients with diabetes mellitus, renal failure or liver failure.

7. Patients or next-of-kin who do not consent to participate in the study. -

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Enteral feeding formula


Locations

Country Name City State
Australia Intensive Care Unit, The Royal Melbourne Hospital, Parkville, Victoria

Sponsors (1)

Lead Sponsor Collaborator
Melbourne Health

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine if high-fat low-carbohydrate enteral feeding reduces the carbon dioxide production and the respiratory quotient in patients with respiratory failure. patients will be followed until death or hospital discharge
Secondary 1. If high-fat, low-carbohydrate enteral feeding reduces carbon dioxide production, dead space ventilation the number of days spent on mechanical ventilation,or the length of ICU stay, hospital length of stay or mortality. patients will be followed until death or hospital discharge
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