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临床试验/NCT01686607
NCT01686607已完成不适用

A Multicenter Cohort Study of the Short and Long-term Safety of Micafungin and Other Parenteral Antifungal Agents

Astellas Pharma Europe B.V.6 个研究点 分布在 1 个国家目标入组 40,110 人开始时间: 2012年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
40,110
试验地点
6
主要终点
Treatment-emergent hepatic injury or dysfunction

研究概览

简要总结

This multicenter observational cohort study proposes to establish the risks of short and long-term outcomes in users of parenteral micafungin and in users of other parenteral antifungal agents from 2005 through 2012 with follow-up until 2017.

详细描述

All eligible patients treated with a parenteral antifungal agent at any time during the years 2005-2012 in each of the participating hospitals, will be included in the study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • hospitalized and treated with parenteral antifungal medication
  • first time treatment of the patient with parenteral antifungal in the medical center was anytime from 2005 through 2012

排除标准

  • prior diagnosis of hepatocellular carcinoma
  • had received parenteral antifungal therapy during the 6 months prior to index hospitalization

研究组 & 干预措施

1) parenteral micafungin users

patients who had been treated with parenteral micafungin

干预措施: Parenteral micafungin application (Drug)

2) other parenteral antifungal users

patients who had been treated with a parenteral antifungal agent (not micafungin)

干预措施: Other parenteral antifungal drugs (Drug)

结局指标

主要结局

Treatment-emergent hepatic injury or dysfunction

时间窗: Up to 30 days after termination of the index treatment

Data will be used of patients treated during the years 2005-2012 with a parenteral antifungal agent in the participating centers.

Treatment-emergent renal failure or dysfunction

时间窗: Up to 30 days after termination of the index treatment

Data will be used of patients treated during the years 2005-2012 with a parenteral antifungal agent in the participating centers.

Rehospitalization for the parenteral treatment of fungal infections

时间窗: Up to 30 days after termination of the index treatment

Data will be used of patients treated during the years 2005-2012 with a parenteral antifungal agent in the participating centers.

Death from hepatocellular carcinoma (HCC)

时间窗: Up to 13 years after treatment

On a long-term basis up to 13 years from 2005-2017.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (6)

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