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Clinical Trial Summary

The objective of this study is to conduct a population pharmacokinetic analysis of caspofungin in a population of patients with moderate and severe acute alcoholic hepatitis or liver disease with Child-Pugh score B and C in order to better characterize pharmacokinetic parameters in case of moderate and severe liver dysfunction.


Clinical Trial Description

patients admitted for alcoholic hepatitis or decompensated cirrhosis and Child-Pugh score 7-9 and 10-15 will be included; all patients without invasive aspergillosis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01968395
Study type Interventional
Source Erasme University Hospital
Contact
Status Completed
Phase Phase 4
Start date September 2013
Completion date October 21, 2014

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