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Trauma Reception and Resuscitation Project

This study has been completed.
Sponsor:
Collaborators:
Victorian Trauma Foundation
National Trauma Research Institute
Information provided by (Responsible Party):
Bayside Health
ClinicalTrials.gov Identifier:
NCT00164034
First received: September 13, 2005
Last updated: February 10, 2013
Last verified: September 2005
History of Changes
  Purpose

Test the hypothesis that the implementation of real-time, computer-prompted algorithms in the first half hour of trauma management will result in a measurable reduction in management errors associated with the reception and resuscitation of major trauma patients.

Demonstrate that a reduction in management errors will translate into a reduction in morbidity and mortality.


Condition Intervention
Trauma
 Device: Real time computer prompted trauma algorithms

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Trauma Reception and Resuscitation Project - 'Time for a New Approach'

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Bayside Health:

Primary Outcome Measures:
  • Error rate per patient treated demonstrated by deviation from the algorithms

Secondary Outcome Measures:
  • Missed injuries
  • Time to decision
Enrollment: 1171
Study Start Date: November 2005
Study Completion Date: November 2008
Primary Completion Date: November 2008 (Final data collection date for primary outcome measure)
  Eligibility
Ages Eligible for Study:   16 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria: All injured patients > 15 years old who are brought or present to the The Alfred Trauma Centre during the study period.

Exclusion Criteria: Stable Trauma patients (ie Pulse rate <100/minute, MAP >70mmHg, Hb >70, temperature >35 and <37.5, Spo2 >92%, GCS >13) undergoing secondary transfer from another hospital, where trauma occurred >6hrs prior to arrival.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00164034

Locations
Australia, Victoria
The Alfred Hospital, Emergency and Trauma Centre, .
Melbourne, Victoria, Australia, 3004
Sponsors and Collaborators
Bayside Health
Victorian Trauma Foundation
National Trauma Research Institute
Investigators
Principal Investigator: Mark Fitzgerald, MBBS, FACEM, MRCMA The Alfred Hospital, Bayside Health, Melbourne, Australia
  More Information

Additional Information:
National Trauma Research Institute  This link exits the ClinicalTrials.gov site
The Alfred Hospital, Melbourne, Victoria, Australia.  This link exits the ClinicalTrials.gov site
The Victorian Trauma Foundation  This link exits the ClinicalTrials.gov site

No publications provided by Bayside Health

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Responsible Party: Bayside Health
ClinicalTrials.gov Identifier: NCT00164034     History of Changes
Other Study ID Numbers: 166/03
Study First Received: September 13, 2005
Last Updated: February 10, 2013
Health Authority: Australia: National Health and Medical Research Council

Keywords provided by Bayside Health:
Trauma
Wounds
Injuries

ClinicalTrials.gov processed this record on March 03, 2015