RecruitingACTRN12605000757617

Trauma Reception and Resuscitation Project - Time for a new approach

A randomised controlled trial comparing trauma resuscitation supported by real time computer prompted algorithms against those without.


Sponsor

Victorian Trauma Foundation

Enrollment

1,162 participants

Start Date

Dec 1, 2005

Study Type

Interventional

Conditions


Eligibility

Sex: Both males and females

Plain Language Summary

Simplified for easier understanding

This study is looking at a new approach to treating trauma patients in the emergency department. Serious injuries from accidents, falls, or violence need fast and organised care. The study compares standard trauma resuscitation (the usual treatment protocol) with a new approach to see if outcomes improve when care is structured differently. You may be eligible if: - You are a stable trauma patient arriving at the Trauma Centre of The Alfred Hospital - You are medically stable at arrival (for example, your heart rate, blood pressure, haemoglobin, temperature, oxygen levels, and consciousness levels are within acceptable ranges) You may NOT be eligible if: - You are being transferred from another hospital (secondary transfer) - Your injury happened more than 6 hours before you arrive at the hospital Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

Trauma resuscitation supported by real time, computer prompted algorithms. 9 month period of data collection during the intervention period.

Trauma resuscitation supported by real time, computer prompted algorithms. 9 month period of data collection during the intervention period.


Locations(1)

Australia

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12605000757617


Related Trials