The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02002013




Registration number
NCT02002013
Ethics application status
Date submitted
28/11/2013
Date registered
5/12/2013
Date last updated
11/03/2015

Titles & IDs
Public title
The Fluid Translation of Research Into Practice Study
Scientific title
The Fluid Translation of Research Into Practice Study (Fluid-TRIPS): An International Cross-Sectional Survey of Fluid Resuscitation Practice
Secondary ID [1] 0 0
ACTRN12613001172796
Secondary ID [2] 0 0
GI-CCT300413
Universal Trial Number (UTN)
Trial acronym
Fluid-TRIPS
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Critical Care, Fluid Resuscitation 0 0
Condition category
Condition code

Intervention/exposure
Study type
Observational
Patient registry
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
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.

Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Type of resuscitation fluid in ICU
Timepoint [1] 0 0
24-hour study day
Secondary outcome [1] 0 0
Cost comparison of fluid choice between regions
Timepoint [1] 0 0
Designated 24-hour study day

Eligibility
Key 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.
Minimum age
16 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Children under 16 years are excluded

Study design
Purpose
Duration
Selection
Timing
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 0 0
The The George Institute for global health; Critical Care & Trauma Division - Sydney
Recruitment postcode(s) [1] 0 0
2000 - Sydney

Funding & Sponsors
Primary sponsor type
Other
Name
The George Institute for Global Health, Australia
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Naomi Hammond
Address 0 0
The George Institute
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

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

No documents have been uploaded by study researchers.