REFACED Sepsis
Title
REFACED Sepsis
Aim
To test if an IV fluid restrictive protocol in ED patients with sepsis is feasible, i.e., if the protocol decreases the IV fluid volumes administered. tration.
Design
An investigator-initiated, multicenter, randomized, parallel-group, open-labeled, feasibility trial investigating volumes of fluid within 24 hours in 124 patients with sepsis allocated to two different IV fluid regimens enrolled at three emergency departments in Central Region Denmark: either standard care arm or fluid-restrictive arm.
Setting
Aarhus University Hospital, Regional Hospital Randers and Regional Hospital Viborg in Central Denmark Region.
Population
Outcome
24-hour intravenous crystalloid fluid administration
Collaborators
Aarhus University Hospital, Randers Regional Hospital and Viborg Regional Hospital.
