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临床试验/JPRN-UMIN000004979
JPRN-UMIN000004979已完成2 期

Efficacy and safety of Garenoxacin for the prevention in the patients with hematological malignancies after chemotherapy - Garenoxacin for the prevention in hematological malignancies

Gifu University Hospital0 个研究点目标入组 50 人开始时间: 2011年1月31日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
16years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)GRNX is obviously ineffective to the pathogen. 2)Patients with a history of allergy/severe adverse effect to quinolone antibacterial agents or garenoxacin 3)Allergic diathesis 4)Pregnancy/lactation 5)Age of 15 years or younger 6)Patient was received systemic antibacterial therapy within 14 days 7)Patients who are regarded as inadequate

研究者

发起方
Gifu University Hospital

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