ID | 62820 |
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Author |
Iwata, Takehiro
Department of Urology, Okayama University Hospital
Kaken ID
Sadahira, Takuya
Department of Urology, Okayama University Hospital
Maruyama, Yuki
Department of Urology, Okayama University Hospital
Sekito, Takanori
Department of Urology, Okayama University Hospital
Yoshinaga, Kasumi
Department of Urology, Okayama University Hospital
Watari, Shogo
Department of Urology, Okayama University Hospital
Nagao, Kentaro
Department of Urology, Okayama University Hospital
Kawada, Tatsushi
Department of Urology, Okayama University Hospital
Tominaga, Yusuke
Department of Urology, Okayama University Hospital
Nishimura, Shingo
Department of Urology, Okayama University Hospital
Takamoto, Atsushi
Department of Urology, Okayama University Hospital
Sako, Tomoko
Department of Urology, Okayama University Hospital
Edamura, Kohei
Department of Urology, Okayama University Hospital
Watanabe, Toyohiko
Department of Urology, Okayama University Hospital
ORCID
Kaken ID
publons
researchmap
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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.
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Keywords | genitourinary tract infections
fluoroquinolone resistance
extended-spectrum beta-lactamase
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Amo Type | Clinical Study Protocol
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Publication Title |
Acta Medica Okayama
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Published Date | 2021-12
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Volume | volume75
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Issue | issue6
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Publisher | Okayama University Medical School
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Start Page | 763
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End Page | 766
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ISSN | 0386-300X
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NCID | AA00508441
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Content Type |
Journal Article
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language |
English
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Copyright Holders | Copyright Ⓒ 2021 by Okayama University Medical School
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File Version | publisher
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Refereed |
True
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