U.S., Sept. 25 -- ClinicalTrials.gov registry received information related to the study (NCT07191054) titled 'LifeFlow Sepsis Study' on April 17, 2019.
Brief Summary: This is a prospective, comparative, blinded, randomized study to prove the safety, efficacy and ease of use of the LifeFlow(R) device in pediatric patients presenting to an emergency department with concern for sepsis. This study will include 600 patients, 300 will receive the LifeFlow(R) device to deliver intravenous fluids while another 300 patients will receive the conventional push/pull method.
Study Start Date: May 01, 2019
Study Type: INTERVENTIONAL
Condition:
Sepsis
Intervention:
DEVICE: LifeFlow Rapid infuser
Use of rapid infuser to fluid resuscitate
DEVICE: P...