Sepsis fluid study pulled before enrolling a single patient
NCT ID NCT07191054
First seen Nov 01, 2025 · Last updated May 09, 2026 · Updated 28 times
Summary
This study was designed to see if a device called LifeFlow® could deliver fluids faster and more safely to children with sepsis in the emergency room compared to the usual push/pull method. It planned to include 600 children under 19 years old, but the study was withdrawn before any participants were enrolled. No results are available.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Phoenix Children's
Phoenix, Arizona, 85016, United States
Conditions
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