- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02002013
The Fluid Translation of Research Into Practice Study (Fluid-TRIPS)
The Fluid Translation of Research Into Practice Study (Fluid-TRIPS): An International Cross-Sectional Survey of Fluid Resuscitation Practice
Study Overview
Status
Conditions
Detailed Description
The Fluid-Translation of Research into Practice Study (TRIPS) is an international, single day, cross-sectional study planned for the second quarter of 2014, coordinated by the George Institute for Global Health, with the purpose of documenting prescribing practices for fluid resuscitation in intensive care units (ICUs) worldwide. This international cross-sectional study follows on from the publication of large-scale randomized controlled trials and meta-analyses of fluid resuscitation, which provide evidence of how fluid resuscitation may affect patient-centered outcomes.
Fluid-TRIPS is a repeat of the Saline versus Albumin for Fluid Evaluation (SAFE)-TRIPS which was an international cross-sectional survey conducted in 2007 that had 391 ICU's participate from 25 countries and provided insight into international fluid resuscitation practice at that time. Along with establishing if fluid resuscitation practices have changed since SAFE-TRIPS, Fluid-TRIPS also aims to determine the relationship between fluid choice and evidence, along with understand other factors that may influence the choice of bolus fluid in clinical practice.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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New South Wales
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Sydney, New South Wales, Australia, 2000
- The The George Institute for global health; Critical Care & Trauma Division
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
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.
Exclusion Criteria:
Children under 16 years are excluded
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Type of resuscitation fluid in ICU
Time Frame: 24-hour study day
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To describe the amount and type of resuscitation fluid currently administered to adult patients in intensive care units (ICU) in different countries
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24-hour study day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cost comparison of fluid choice between regions
Time Frame: Designated 24-hour study day
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To describe and compare the costs of fluid choice between different geographical regions
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Designated 24-hour study day
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Collaborators and Investigators
Investigators
- Study Chair: Naomi Hammond, The George Institute
- Study Chair: Colman Taylor, The George Institute
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- GI-CCT300413
- ACTRN12613001172796 (OTHER: Australian New Zealand Clinical Trials Registry)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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