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DEFINITIONS
Trial Review
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Trial registered on ANZCTR
Registration number
ACTRN12615000031561
Ethics application status
Approved
Date submitted
11/12/2014
Date registered
19/01/2015
Date last updated
8/11/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
The Fluid Translation of Research into Practice Study - Discrete Choice Experiment (Survey) of Intensive Care clinicians preferences of resuscitation fluid.
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Scientific title
Discrete choice experiment to understand what drives intensive care clinicians' choice of fluid type used for fluid resuscitation in intensive care patients
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Secondary ID [1]
285817
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
Fluid TRIPS DCE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Critical Illness
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Hypovolemia
293721
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Fluid resuscitation
293722
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Condition category
Condition code
Public Health
294022
294022
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0
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Health service research
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
The aim of this study is to define and understand the fundamental drivers of fluid resuscitation choice for critically ill patients. The study uses a scenario based survey of clinician preferences using the Discrete Choice Experiment (DCE) methodology. The survey will be administered online via a secure database and will take each clinician approximately 20-30 minutes to complete. The study period is anticipated to run for 2-3 months.
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Intervention code [1]
290789
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Not applicable
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Comparator / control treatment
Not applicable
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The primary objective of this study is to identify key attributes that have the largest influence on the choice of fluid used for resuscitation.
The statistical analysis of the DCE data will involve a mixed multinomial (randoms parameters) logit model (MMNL) using a panel size specification.
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Assessment method [1]
293799
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Timepoint [1]
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Within 6 months of completion of the Fluid TRIPS Study
Australian New Zealand Clinical Trials Registry, Number:ACTRN12613001172796
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Secondary outcome [1]
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The secondary objective is to describe a “willingness to spend” threshold (by international region) where clinicians will switch from less expensive preparations to more expensive preparations.
The analysis will enable: 1) estimates of the marginal effect of each attribute, and respondent characteristic on choice of resuscitation fluid; 2) the relative tradeoff (or marginal rate of substitution) between attributes, in particular the calculation of clinician “willingness to spend” thresholds, and 3) predictions to be made of the preference for current resuscitation fluids.
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Assessment method [1]
311899
0
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Timepoint [1]
311899
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Within 6 months of completion of the Fluid TRIPS Study Australian New Zealand Clinical Trials Registry, Number:ACTRN12613001172796
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Eligibility
Key inclusion criteria
Intensive Care Clinician at participating hospital
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Minimum age
No limit
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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?
Yes
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Key exclusion criteria
Nil
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Study design
Purpose
Screening
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Duration
Cross-sectional
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Selection
Convenience sample
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Timing
Prospective
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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
16/03/2015
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Actual
14/08/2015
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Date of last participant enrolment
Anticipated
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Actual
30/12/2015
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Date of last data collection
Anticipated
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Actual
29/02/2016
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Sample size
Target
352
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Accrual to date
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Final
367
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,TAS,WA,VIC
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Recruitment outside Australia
Country [1]
6517
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New Zealand
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State/province [1]
6517
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Country [2]
6518
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Brazil
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State/province [2]
6518
0
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Country [3]
6519
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Belgium
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State/province [3]
6519
0
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Country [4]
6520
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Canada
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State/province [4]
6520
0
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Country [5]
6521
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Chile
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State/province [5]
6521
0
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Country [6]
6522
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France
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State/province [6]
6522
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Country [7]
6523
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Germany
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State/province [7]
6523
0
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Country [8]
6524
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Ireland
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State/province [8]
6524
0
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Country [9]
6525
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Italy
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State/province [9]
6525
0
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Country [10]
6526
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Japan
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State/province [10]
6526
0
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Country [11]
6527
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Monaco
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State/province [11]
6527
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Country [12]
6528
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Singapore
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State/province [12]
6528
0
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Country [13]
6529
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South Africa
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State/province [13]
6529
0
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Country [14]
6530
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United Arab Emirates
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State/province [14]
6530
0
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Country [15]
6531
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Switzerland
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State/province [15]
6531
0
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Country [16]
6532
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United States of America
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State/province [16]
6532
0
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Country [17]
6534
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China
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State/province [17]
6534
0
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Country [18]
6535
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Denmark
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State/province [18]
6535
0
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Country [19]
6536
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Hong Kong
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State/province [19]
6536
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Country [20]
6537
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Sweden
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State/province [20]
6537
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Funding & Sponsors
Funding source category [1]
290377
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Other Collaborative groups
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Name [1]
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The George Institute for Global Health
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Address [1]
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L13, 321 Kent Street
Sydney NSW 2000
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Country [1]
290377
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Australia
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Primary sponsor type
Other Collaborative groups
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Name
The George Institute for Global Health
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Address
L13, 321 Kent Street
Sydney NSW 2000
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Country
Australia
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Secondary sponsor category [1]
289204
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None
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Name [1]
289204
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Address [1]
289204
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Country [1]
289204
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Other collaborator category [1]
278266
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Charities/Societies/Foundations
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Name [1]
278266
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Intensive Care Foundation
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Address [1]
278266
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Level 2, 10 Ievers Terrace
Carlton South
VIC AUSTRALIA 3053
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Country [1]
278266
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
292097
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Sydney Local Health District Ethics Review Committee (RPAH Zone)
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Ethics committee address [1]
292097
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Research Development Office Suite 210A RPAH Medical Centre 100 Carillon Avenue NEWTOWN NSW 2042
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Ethics committee country [1]
292097
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Australia
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Date submitted for ethics approval [1]
292097
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08/01/2015
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Approval date [1]
292097
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08/05/2015
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Ethics approval number [1]
292097
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EC00152
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Summary
Brief summary
Hypotheses: The choice of fluid resuscitation preparations selected by clinicians is determined by short term considerations such as time to haemodynamic benefit and fluid volume required rather than by level of evidence, risk of adverse events or cost. Objectives: The primary objective of this study is to identify the attributes that have the largest influence on the choice of fluid used for resuscitation. The secondary objective is to describe a “willingness to spend” threshold (by international region) where clinicians will switch from less expensive preparations to more expensive preparations.
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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
53390
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Dr Colman Taylor
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Address
53390
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The George Institute for Global Health
L13,321 Kent Street
Sydney NSW 2000
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Country
53390
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Australia
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Phone
53390
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+61 2 9657 0316
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Fax
53390
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Email
53390
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[email protected]
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Contact person for public queries
Name
53391
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Colman Taylor
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Address
53391
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The George Institute for Global Health
L13,321 Kent Street
Sydney NSW 2000
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Country
53391
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Australia
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Phone
53391
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+61 2 9657 0316
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Fax
53391
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Email
53391
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[email protected]
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Contact person for scientific queries
Name
53392
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Colman Taylor
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Address
53392
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The George Institute for Global Health
L13,321 Kent Street
Sydney NSW 2000
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Country
53392
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Australia
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Phone
53392
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+61 2 9657 0316
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Fax
53392
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Email
53392
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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
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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