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Trial registered on ANZCTR
Registration number
ACTRN12611000793910
Ethics application status
Approved
Date submitted
27/07/2011
Date registered
28/07/2011
Date last updated
3/12/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
The Augmented versus Routine approach to Giving Energy Trial (TARGET): A feasibility trial in the critically ill
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Scientific title
The Augmented versus Routine approach to Giving Energy Trial (TARGET): A feasibility trial in the critically ill
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Secondary ID [1]
262724
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Nil
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Universal Trial Number (UTN)
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Trial acronym
TARGET
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Energy requirement in the critically ill
270433
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Condition category
Condition code
Diet and Nutrition
270579
270579
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0
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Other diet and nutrition disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
1.5 kilocalorie per ml enteral feed formulation delivered via naso-gastric tube at a goal rate of 1ml per kilogram per hour (capped at 100ml/hr) continuously for a maximum of 10 days. Blinded enteral nutrition will cease prior to day 10 if one of the following occur: cessation of enteral nutrition by the treating clinicians, patient is discharged from the ICU, treating clinician decides that it is in the patients best interest to cease the study intervention or informed consent is withdrawn.
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Intervention code [1]
267071
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Treatment: Other
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Comparator / control treatment
1.0 kilocalorie per ml enteral feed formulation delivered via naso-gastric tube at a goal rate of 1ml per kilogram per hour (capped at 100ml/hr) continuously for a maximum of 10 days. Blinded enteral nutrition will cease prior to day 10 if one of the following occur: cessation of enteral nutrition by the treating clinicians, patient is discharged from the ICU, treating clinician decides that it is in the patients best interest to cease the study intervention or informed consent is withdrawn.
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Control group
Active
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Outcomes
Primary outcome [1]
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To determine whether the administration of the treatment enteral feed (1.5 kcal/ml) increases mean daily energy delivery (kilocalorie per day) by > or equal to 20% compared to the control (1.0 kcal/ml). Energy delivery = calorie concentration of the feed X (volume delivered - gastric residual volume discarded)
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Assessment method [1]
269321
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Timepoint [1]
269321
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Study enteral formula administered for up to 10 days. Mean daily energy delivered calculated over/ up to the 10 day treatment period.
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Secondary outcome [1]
279372
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Mortality
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Assessment method [1]
279372
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Timepoint [1]
279372
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90 days
Hospital
Intensive Care Unit
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Secondary outcome [2]
279373
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Length of Stay recorded in time units (days) obtained from electronic admission databases and medical records
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Assessment method [2]
279373
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Timepoint [2]
279373
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Hospital: admission to discharge in days
Intensive Care Unit: admission to discharge in days
Assessed at discharge
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Secondary outcome [3]
279374
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Invasive Mechanical Ventilator free days
Assessed at day 28: number of days patient off the invasive mechanical ventilator (equipment) collated. ICU observation flow charts used as source data to obtain information
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Assessment method [3]
279374
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Timepoint [3]
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28 days
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Eligibility
Key inclusion criteria
Invasive mechanically ventilated critically ill patients
Expected intensive care unit stay > or = to 3 days
Suitable for, or receiving (within 12 hours) enteral nutrition.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Expected death within 24 hours
Patient not for active treatment
Target enteral feed volume contraindicated
Requirement for specific nutritional therapy other than study enteral formulation.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Patients admitted to participating centre intensive care units will be screened for potential recruitment to the study. Eligible subjects enrolled by intensive care nursing, medical and dietician staff. Central randomisation via computer/ website. Following randomisation to either 1 kcal/ml or 1.5 kcal/ml pre -numbered blinded/ masked (with an enclosed opaque coloured plastic casing) enteral feed (boxed in groups of 6) will be allocated to subjects via the study website feed allocation web page. Nursing staff will locate the correct numbered enteral nutrition box from the store and assign to the study subject. Feed type concealed by covering the feed container and allocation concealment achieved/ maintained.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computerised permuted block randomisation method with variable block sizes, stratified by centre in a 1:1 ratio.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
30/08/2011
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Actual
24/01/2013
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Date of last participant enrolment
Anticipated
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Actual
4/05/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
112
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
4320
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5000
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Recruitment postcode(s) [2]
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5011
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Recruitment postcode(s) [3]
4322
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2605
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Recruitment postcode(s) [4]
4324
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2050
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Recruitment postcode(s) [5]
4325
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3084
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Funding & Sponsors
Funding source category [1]
267544
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Hospital
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Name [1]
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Royal Adelaide Hospital
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Address [1]
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North Terrace
Adelaide
South Australia 5000
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Country [1]
267544
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Australia
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Funding source category [2]
287908
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Other Collaborative groups
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Name [2]
287908
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Australian and New Zealand College of Anaesthetists
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Address [2]
287908
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630 St Kilda Road
Melbourne Vic 3004
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Country [2]
287908
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Australia
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Primary sponsor type
Individual
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Name
Dr Marianne Chapman
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Address
Intensive Care Unit
Royal Adelaide Hospital
North Terrace
Adelaide
South Australia 5000
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Country
Australia
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Secondary sponsor category [1]
266581
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Individual
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Name [1]
266581
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Dr Sandra Peake
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Address [1]
266581
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Department of Intensive Care
The Queen Elizabeth Hospital
1st Floor Main Building
28 Woodville Road,
Woodville
South Australia 5011
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Country [1]
266581
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Australia
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Secondary sponsor category [2]
266582
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Individual
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Name [2]
266582
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Dr Andrew Davies
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Address [2]
266582
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Intensive Care Unit
Alfred Hospital
Commercial Road
Melbourne
Victoria 3004
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Country [2]
266582
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Australia
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Secondary sponsor category [3]
286635
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Individual
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Name [3]
286635
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Stephanie O'Connor
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Address [3]
286635
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Intensive Care Unit Royal Adelaide Hospital North Terrace Adelaide South Australia 5000
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Country [3]
286635
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Australia
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Secondary sponsor category [4]
286636
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Individual
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Name [4]
286636
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Emma Ridley
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Address [4]
286636
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Department of Epidemiology & Preventive Medicine
Monash University
The Alfred Centre
99 Commercial Road
Melbourne Vic 3004
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Country [4]
286636
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Australia
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Secondary sponsor category [5]
286637
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Individual
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Name [5]
286637
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Patricia Williams
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Address [5]
286637
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C/O The Queen Elizabeth Hospital
Intensive Care Unit
28 Woodville Rd
Woodville
South Australia 5011
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Country [5]
286637
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Australia
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Secondary sponsor category [6]
287070
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Individual
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Name [6]
287070
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Adam M Deane
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Address [6]
287070
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Intensive Care Unit
Critical Care Services
Royal Adelaide Hospital
North Terrace, Adelaide, SA 5000
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Country [6]
287070
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
269501
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Royal Adelaide Hospital Research Ethics Committee
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Ethics committee address [1]
269501
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Level 3 Hanson Institute Royal Adelaide Hospital North Terrace Adelaide South Australia 5000
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Ethics committee country [1]
269501
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Australia
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Date submitted for ethics approval [1]
269501
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30/11/2010
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Approval date [1]
269501
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14/03/2011
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Ethics approval number [1]
269501
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101218
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Summary
Brief summary
This trial is a feasibility/ pilot study to establish if the administration of the treatment enteral feed (1.5 kcal/ml) increases mean daily energy delivery (kilocalorie per day) by > or equal to 20% compared to the control (1.0 kcal/ml). The study will provide baseline data to allow for the planning and funding of a larger multi centre trial to determine if delivery of additional energy to critically ill adults over the first 10 days of their ICU stay affects clinically important outcomes. Following the 10 day study treatment period, if required, patients in both groups will receive additional nutrition according to the centres standard care. The pilot study will be conducted in 6 centres in Australia with 100 patients enrolled over a six month period.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
32942
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A/Prof Marianne Chapman
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Address
32942
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Department of Acute Care Medicine
University of Adelaide
Royal Adelaide Hospital
North Terrace
Level 5, Eleanor Harrald Building
Adelaide
South Australia 5000
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Country
32942
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Australia
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Phone
32942
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+61 412 183 894
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Fax
32942
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Email
32942
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[email protected]
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Contact person for public queries
Name
16189
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Sandra Peake
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Address
16189
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Department of Intensive Care
The Queen Elizabeth Hospital
1st Floor Main Building
28 Woodville Road,
Woodville 5011
South Australia
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Country
16189
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Australia
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Phone
16189
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+61 8 8222 6000
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Fax
16189
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Email
16189
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[email protected]
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Contact person for scientific queries
Name
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Marianne Chapman
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Address
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Director of Research/ Senior Staff Specialist
Intensive Care
Department of Critical Care Services
Royal Adelaide Hospital
North Terrace
Adelaide 5000
South Australia
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Country
7117
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Australia
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Phone
7117
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+61 8 8222 4000
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Fax
7117
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Email
7117
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Plain language summary
No
Patients were randomised to receive 1.5 (n=57) or ...
[
More Details
]
Study results article
Yes
Peake SL, Davies AR, Deane AM, Lange K, Moran JL, ...
[
More Details
]
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Use of a concentrated enteral nutrition solution to increase calorie delivery to critically ill patients: A randomized, double-blind, clinical trial.
2014
https://dx.doi.org/10.3945/ajcn.114.086322
N.B. These documents automatically identified may not have been verified by the study sponsor.
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