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Characterization of the Efficacy of Furosemide Depending on Albumin Function

Critical Illness Clinical Trial

Official title:
Characterization of the Efficacy of Furosemide Depending on Albumin Function - a Prospective Monocentric Observational Study

Clinical Trial Summary

During this prospective, uncontrolled and non-interventional observational study, the influence of albumin function on the efficacy of furosemide will be investigated. The aim of the study is to provide information on the efficacy of furosemide depending on albumin function.

Clinical Trial Description

In patients with intravenous furosemide administration, an additional 15 ml of blood is taken for the analysis of specific parameters as part of the blood sampling necessary for the treatment of the patient. The effect of furosemide is assessed on the basis of the patient's urine excretion. For this purpose, fluid intake and excretion are balanced over 6 hours. The blood sample is taken at the beginning of the balancing period. In addition, the albumin concentration, ABiC, as well as the total and free concentration of furosemide in the collected urine are determined. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04972617
Study type Observational
Source University of Rostock
Contact
Status Completed
Phase
Start date May 17, 2022
Completion date October 31, 2022
View Details
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