LifeFlow Sepsis Study

Withdrawn before enrolling · Not applicable

Conditions studied: Sepsis

In brief

This is a prospective, comparative, blinded, randomized study to prove the safety, efficacy and ease of use of the LifeFlow® device in pediatric patients presenting to an emergency department with concern for sepsis. This study will include 600 patients, 300 will receive the LifeFlow® device to deliver intravenous fluids while another 300 patients will receive the conventional push/pull method.

Key facts

Study ID

NCT07191054

Run by

Phoenix Children's Hospital

People needed

0

Starts

2019-05-01

Expected to finish

2020-03-30

Last updated by the study team

2025-09-24

Who can join

Age: 1 and older, up to 19. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Less than 19 years old
• Trigger the Best Practice Alert in triage
• Treating physician elects to do the full sepsis bundle.

You may not qualify if…

• Less than 20kg in weight
• Patients on diuretics for cardiac or renal conditions
• Patients who cannot communicate in either English or Spanish

Where it is running

• Phoenix Children's — Phoenix, Arizona, United States

Full record on ClinicalTrials.gov

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