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NCT00164034 Clinical Trial

Trauma Reception and Resuscitation Project

Trauma Clinical Trial

Official title:
Trauma Reception and Resuscitation Project - 'Time for a New Approach'

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00164034
Other study ID # 166/03
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated February 10, 2013
Start date November 2005
Est. completion date November 2008

Study information
Verified date September 2005
Source Bayside Health
Contact n/a
Is FDA regulated No
Health authority Australia: National Health and Medical Research Council
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 1171
Est. completion date November 2008
Est. primary completion date November 2008
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility 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.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Device:
• Real time computer prompted trauma algorithms

Locations
Country Name City State
Australia The Alfred Hospital, Emergency and Trauma Centre, . Melbourne Victoria

Sponsors (3)
Lead Sponsor Collaborator
Bayside Health National Trauma Research Institute, Victorian Trauma Foundation

Country where clinical trial is conducted

Australia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Error rate per patient treated demonstrated by deviation from the algorithms
Secondary Missed injuries
Secondary Time to decision
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