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Trial registered on ANZCTR
Registration number
ACTRN12607000462482
Ethics application status
Approved
Date submitted
31/08/2007
Date registered
12/09/2007
Date last updated
18/11/2019
Date data sharing statement initially provided
18/11/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Fluid Responsiveness in Septic Shock
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Scientific title
To assess the change in cardiac output from clinical fluid challenge in patients with septic shock.
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Septic shock.
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Condition category
Condition code
Cardiovascular
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Other cardiovascular diseases
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Intervention/exposure
Study type
Observational
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Patient registry
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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
Clinically administered fluid challenge (250mL colloid intravenous infusion over 15 minutes at request of treating clinician).
Participation in each study will take approximately 30 minutes of participant time.
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Intervention code [1]
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Not applicable
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Comparator / control treatment
Nil.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Correlation between baseline variables and subsequent increase in cardiac output (measured by USCOM).
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Assessment method [1]
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Timepoint [1]
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Immediateley before and after fluid challenge.
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Secondary outcome [1]
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Increase in cardiac output (measured by USCOM) of equal to or greater than 15%.
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Assessment method [1]
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Timepoint [1]
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Immediately after fluid challenge.
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Eligibility
Key inclusion criteria
Intensive care unit patients diagnosed with septic shock where fluid challenge is clinically requested.
Septic shock will be defined in terms of the International Sepsis Definitions Conference [American College of Chest Physicians/Society of Critical Care Medicine
Consensus Conference: definitions for sepsis and organ failure and guidelines
for the use of innovative therapies in sepsis. Crit Care Med 1992;20(6):864-74].
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Minimum age
18
Years
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Maximum age
N/A
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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
Treating clinician or patient/legally authorised representative decline participation/consent. Age <18 years at time of eligibility, presence of moderate to severe valve disease, evidence of fluid overload (such as impaired gas exchange or radiographic evidence of pulmonary oedema).
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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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
31/08/2007
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Actual
1/09/2007
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Date of last participant enrolment
Anticipated
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Actual
31/12/2007
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Date of last data collection
Anticipated
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Actual
31/12/2007
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Sample size
Target
10
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Accrual to date
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Final
10
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Other
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Name [1]
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Australian And New Zealand College of Anaesthetists
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Address [1]
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Australian And New Zealand College of Anaesthetists (ANZCA) House
630 St Kilda Road
Melbourne VIC 3004
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Country [1]
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Australia
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Primary sponsor type
University
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Name
University of Queensland
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Address
The University of Queensland
Brisbane QLD 4072
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Country
Australia
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Wesley Hospital
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Address [1]
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451 Coronation Drive
Auchenflower QLD 4066
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Uniting Healthcare Human Research Ethics Committee
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Ethics committee address [1]
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451 Coronation Drive Auchenflower QLD 4066
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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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Approval date [1]
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22/06/2007
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Ethics approval number [1]
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2007/36
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Summary
Brief summary
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Trial website
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Trial related presentations / publications
A comparison of transcutaneous Doppler corrected flow time, b-type natriuretic peptide and central venous pressure as predictors of fluid responsiveness in septic shock: a preliminary evaluation. Sturgess DJ, Pascoe RL, Scalia G, Venkatesh B. Anaesth Intensive Care. 2010 Mar;38(2):336-41.
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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 David Sturgess
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Address
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451 Coronation Drive
Auchenflower QLD 4066
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Country
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Australia
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Phone
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+61 7 32327000
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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 David Sturgess
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Address
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451 Coronation Drive
Auchenflower QLD 4066
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Country
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Australia
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Phone
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+61 7 32327000
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Fax
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
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No/undecided IPD sharing reason/comment
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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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