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• W4200317418 abstract "The aim of this ongoing trial is to evaluate the clinical efficacy and safety of sitafloxacin (STFX) 200 mg once daily (QD) for 7 days in patients with refractory genitourinary tract infections, which include recurrent or complicated cystitis, complicated pyelonephritis, bacterial prostatitis, and epididymitis. The primary endpoint is the microbiological efficacy at 5-9 days after the last administration of STFX. Recruitment began in February 2021, and the target total sample size is 92 participants." @default.
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• W4200317418 date "2021-12-01" @default.
• W4200317418 modified "2023-09-29" @default.
• W4200317418 title "Clinical Efficacy and Safety of Sitafloxacin 200 mg Once Daily for Refractory Genitourinary Tract Infections." @default.
• W4200317418 doi "https://doi.org/10.18926/amo/62820" @default.
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