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Fluid Administration and Fluid Overload in the Intensive Care Unit — FLUID-ICU  

Fluid Overload Clinical Trial

Official title:
Fluid Administration and Fluid Overload in the Intensive Care Unit (FLUID-ICU) - an International Inception Cohort Study

Clinical Trial Summary

The goal of this international inception cohort study is to describe fluid administration during admittance to the intensive care unit (ICU), and provide contemporary epidemiological data on fluid overload, risk factors, management and outcome in critically ill adult patients.

Clinical Trial Description

Background: Fluid overload is associated with adverse outcome in ICU patients, however, assessment of fluid status is often difficult and no established definition and consistent detection method exists. Former research has primarily focused on the use of resuscitation fluid, but a substantial amount of fluid is administered throughout the entire ICU stay and this fluid may be a clinically relevant source of fluid overload. Objectives: To describe fluid administration practices during the entire ICU stay, and provide contemporary epidemiological data on fluid overload, fluid removal, risk factors and association with patient outcomes from a worldwide perspective. Study design: International inception cohort study. Patients will be included during a 14-day inception period to be chosen by each participating site. Population: Critically ill adult patients (≥ 18 years) with acute admission to the ICU. Intervention: None. Only routinely available data will be collected. Study duration: Patients are followed daily until ICU discharge or death for a maximum of 28 days. Follow-up is performed 90 days after ICU admission. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06258616
Study type Observational [Patient Registry]
Source Nordsjaellands Hospital
Contact Clara Molin, MD, PhD student
Phone +4528683965
Email claramolinmolin@gmail.com
Status Recruiting
Phase
Start date April 2024
Completion date August 2025
View Details
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