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Clinical Trial Summary

The purpose of the study is to investigate the role of the human immune response to candidemia/invasive candidiasis as it relates to the cytokine interferon-gamma.


Clinical Trial Description

In this study, patients with Candida bloodstream infection, peritonitis/intra-abdominal abscess, and pleural empyema will be enrolled. Persistent candidiasis confirmed by culture will be defined as follows: (i) Candida bloodstream infection present for >48 hours after initiation of effective antifungal treatment and after removal of intravenous devices, (ii) Intra-abdominal infection (peritonitis or abscess) that persists for >96 hours after source control intervention and effective antifungal treatment, (iii) Pleural empyema that persists for >96 hours after placement of drainage catheter and effective antifungal treatment. Outcomes in patients with and without persistent candidiasis will be assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05235711
Study type Observational
Source Mayo Clinic
Contact Bjerke Jacob
Phone 507-255-8464
Email bejrke.jacob@mayo.edu
Status Recruiting
Phase
Start date February 10, 2022
Completion date August 2024

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