NCT02002013

Brief Summary

Translating reliable evidence on fluid resuscitation of intensive care patients into clinical practice - Improving patient outcomes and containing public health costs

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2014

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 28, 2013

Completed
7 days until next milestone

First Posted

Study publicly available on registry

December 5, 2013

Completed
4 months until next milestone

Study Start

First participant enrolled

April 1, 2014

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2014

Completed
Last Updated

March 11, 2015

Status Verified

March 1, 2015

Enrollment Period

8 months

First QC Date

November 28, 2013

Last Update Submit

March 9, 2015

Conditions

Critical Care, Fluid Resuscitation

Keywords

AdultICU patientFluid resuscitationobservational study

Outcome Measures

Primary Outcomes (1)

  • Type of resuscitation fluid in ICU

    To describe the amount and type of resuscitation fluid currently administered to adult patients in intensive care units (ICU) in different countries

    24-hour study day

Secondary Outcomes (1)

  • Cost comparison of fluid choice between regions

    Designated 24-hour study day

Study Arms (1)

Adult ICU patient receiving Fluid resus

Adult patients present in the ICU at the start of the study day or admitted during the 24-hour study period will be included in the study sample.

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients present in the ICU on the study day

You may qualify if:

  • Adult patients present in the ICU on the study day or admitted during the 24-hour study period will be included in the study sample.

You may not qualify if:

  • Children under 16 years are excluded

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The The George Institute for global health; Critical Care & Trauma Division

Sydney, New South Wales, 2000, Australia

Location

Related Publications (1)

  • Hammond NE, Taylor C, Finfer S, Machado FR, An Y, Billot L, Bloos F, Bozza F, Cavalcanti AB, Correa M, Du B, Hjortrup PB, Li Y, McIntryre L, Saxena M, Schortgen F, Watts NR, Myburgh J; Fluid-TRIPS and Fluidos Investigators; George Institute for Global Health, The ANZICS Clinical Trials Group, BRICNet, and the REVA research Network. Patterns of intravenous fluid resuscitation use in adult intensive care patients between 2007 and 2014: An international cross-sectional study. PLoS One. 2017 May 12;12(5):e0176292. doi: 10.1371/journal.pone.0176292. eCollection 2017.

    PMID: 28498856DERIVED

Study Officials

  • Naomi Hammond

    The George Institute

    STUDY CHAIR

  • Colman Taylor

    The George Institute

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Co-principle investigator

Study Record Dates

First Submitted

November 28, 2013

First Posted

December 5, 2013

Study Start

April 1, 2014

Primary Completion

December 1, 2014

Study Completion

December 1, 2014

Last Updated

March 11, 2015

Record last verified: 2015-03

Locations

AU(1)