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Clinical Trial Summary

The ProDEms-trial focuses on nurses and ambulance drivers working in prehospital care, taking care on the one hand of patients suffering from time-sensitive critical conditions like STEMI, acute stroke or severe traumatic brain injury, and on the other hand of patients whose lives are not in immediate danger but suffer from acute exacerbation of chronic conditions or suffer from acute pain. In the current study the investigators will use a multistage approach to test the hypothesis whether the use of a CDSS in prehospital emergency care will: 1. Improve protocol adherence, 2. Reduce emergency department length of stay, 3. Improves diagnostic accuracy; without impeding the workflow of the prehospital team or impairing patient safety.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02365792
Study type Interventional
Source KU Leuven
Contact
Status Withdrawn
Phase N/A
Start date June 2016
Completion date December 2025

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