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Clinical Trial Summary

PK of Caspofungin in ICU septic patients might be changed as compared to healthy volunteers due to sepsis-related pathophysiology.

Sub-optimal plasma and tissue concentrations might be achieved in these patients when drugs are administered at the same dosage/regimen suggested for healthy volunteers.


Clinical Trial Description

Open non randomized, non controlled single center study on the pharmacokinetics of caspofungin in 20 consecutive ICU patients with severe sepsis or septic shock, requiring caspofungin therapy and PK-PD evaluation for the optimization of caspofungin therapy. The aim of this study is to describe the Caspofungin PK-PD alterations in a cohort of critically ill septic patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03798600
Study type Observational
Source Careggi Hospital
Contact
Status Completed
Phase
Start date January 1, 2016
Completion date December 31, 2018

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