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Trial registered on ANZCTR
Registration number
ACTRN12608000486325
Ethics application status
Approved
Date submitted
18/08/2008
Date registered
30/09/2008
Date last updated
13/07/2011
Type of registration
Prospectively registered
Titles & IDs
Public title
A randomised controlled trial of non-invasive cardiac output monitoring in the emergency room:
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Scientific title
A randomised controlled trial of non-invasive cardiac output monitoring on oxygen delivery in critically ill emergency department patients.
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Secondary ID [1]
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Nil
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Universal Trial Number (UTN)
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Trial acronym
The NICER TRial
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Critical illness in the emergency department requiring urgent administration of at least 500ml intravenous fluid
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Condition category
Condition code
Cardiovascular
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0
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Diseases of the vasculature and circulation including the lymphatic system
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Subjects will be allocated to standard care plus non-invasive cardiac output monitoring (intervention).
Non-invasive cardiac output monitoring for four hours in the Emergency Department (ED).
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Intervention code [1]
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Early detection / Screening
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Comparator / control treatment
Standard care for the presenting illness without cardiac output monitoring.
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Control group
Active
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Outcomes
Primary outcome [1]
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Lactate levels as measured by blood gas analysis
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Assessment method [1]
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Timepoint [1]
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Four hours post enrollment
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Primary outcome [2]
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Base excess as measured by blood gas analysis
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Assessment method [2]
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Timepoint [2]
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Four hours post enrollment
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Primary outcome [3]
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Vital signs (heart rate and blood pressure)
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Assessment method [3]
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Timepoint [3]
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Four hours post enrollment
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Secondary outcome [1]
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Questionnaire regarding clinicians management plans for each patient, before and after cardiac output monitoring.
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Assessment method [1]
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Timepoint [1]
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Four hours post enrollment
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Eligibility
Key inclusion criteria
Critically ill adults in the ED requiring referral to Intensive Care for consideration of admission.
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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
Age < 18
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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 requiring urgent fluid administration will be randomised to having this guided by non-invasive cardiac output monitoring where stroke volume variation will be used to guide resuscitation or to standard care
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Allocation will be by computerized random number generation
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Masking / blinding
Open (masking not 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
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/11/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
222
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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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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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Queensland Emergency Medicine Research Foundation
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Address [1]
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Suite 5B, The Terrace Suites, 19 Lang Parade, Milton Qld 4064
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Ogilvie Thom
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Address
Box Hill Hospital
Nelson Road
Box Hill
Vic 3128
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Human research Ethics Committee
The Prince Charles Hospital
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Ethics committee address [1]
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Rode Road, Chermside, QLD 4032
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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17/03/2010
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Approval date [1]
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Ethics approval number [1]
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HREC/10/QPCH/16
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Summary
Brief summary
Critically ill patients often have signs of inadequate oxygen delivery. We know this adversely impacts on survival. The hypothesis is that the introduction of non invasive cardiac output monitoring will allow us to improve or correct oxygen delivery, thus possibly improving survival
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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
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Ogilvie Thom
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Address
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Emergency Department, Princess Alexandra Hospital, Ipswich road, Wolloongabba, QLD
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Country
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Australia
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Phone
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(03) 9895 3333
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Ogilvie Thom
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Address
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Emergency Department, Princess Alexandra Hospital, Ipswich road, Wolloongabba, QLD
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Country
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Australia
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Phone
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(03) 9895 3333
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Fax
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Email
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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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