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Clinical Trial Summary

The goal of this quality improvement study is to measure the impact of incorporation of a manual rapid fluid infuser (RFI) for intravenous crystalloid infusion in patients with suspected sepsis in the prehospital interval. The main question[s] it aims to answer are: - Does the intervention affect the timeliness of fluid administration? - Does the intervention affect CMS sepsis bundle care measure compliance? - Does the intervention affect processes and outcomes of care? - Are there any adverse effects? Researchers will compare this intervention to use of more conventional gravity or pressure-infusion bag crystalloid infusion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05961137
Study type Interventional
Source Orange Park Medical Center
Contact
Status Completed
Phase N/A
Start date April 1, 2021
Completion date August 31, 2022

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