Stopped: Insufficient rate of accrual due to the start of a concomitant similar study
This is a multicenter, prospective, open-label, randomized trial. Patients with severe abdominal condition developing severe sepsis or septic shock and receiving broad spectrum antibiotic and antifungal treatment will be randomized (1:1) to: 1. discontinue antifungal treatment based on negative (\<80 pg/ml) result of 1,3 beta-d-glucan performed on day 0,3,6 and 10 2. continue antifungal treatment according with attending physician's decision.
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Antifungal consumption
Timeframe: 28 days
Mortality
Timeframe: 28 days
Length of stay
Timeframe: 28 days