This is a multi-center, prospective, open, observational and optimal clinical research to evaluate the clinical effectiveness and safety of different doses of micafungin sodium for injection in patients with hematological tumors.
This is a multi-center, prospective, open, observational and optimal clinical research to evaluate the clinical effectiveness and safety of different doses of micafungin sodium for injection in patients with hematological tumors. Researchers screened suitable subjects according to the admission criteria, and after signing the informed consent form, micafungin sodium for injection was used for preventive or empirical treatment. During the treatment period, subjects who need to change the treatment plan due to uncontrollable infection or other reasons will withdraw from this research and the researchers will decide the follow-up treatment plan.All subjects were monitored for efficacy and safety according to the visit plan during the research.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
230
micafungin sodium ≥ 100, \<200mg/time, once a day, intravenous drip. Low dose group
Department of Hematology, Provincial Hospital Affiliated to Shandong University
Jinan, Shandong, China
RECRUITINGclinical efficacy
Breakthrough incidence of Invasive Fungal Infection (IFI), during prophylaxis use of micafungin
Time frame: 14 days
Safety assessed by lab-test and adverse events
Incidence of adverse reactions in different dose groups of micafungin
Time frame: 30 days
Survival rate
IFD-related mortality
Time frame: 30 days
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