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临床试验/NCT01706562
NCT01706562已完成不适用

Retrospective Observation of Empirical Antifungal Therapy With Itraconazole

Janssen Korea, Ltd., Korea0 个研究点目标入组 138 人开始时间: 2011年5月最近更新:
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
138
主要终点
Success rate of itraconazole treatment when used for more than 7 days

研究概览

简要总结

The purpose of this study is to investigate the overall success rate of itraconazole intravenous treatment for a period of more than 7 days.

详细描述

This is a retrospective study ie, a study that looks backward in time, usually using medical records and interviews with patients who are already known to have a disease, in patients with itraconazole intravenous prescription as an empirical (based on practical experience) antifungal agent. This study collects baseline information about underlying disease, sign of fungal infection, neutropenia (a decrease in white blood cells), neutropenic fever duration and the reason for discontinuation. Neutropenia is defined as a neutrophil (white blood cell) count of ≤500 cells/mm3 or a count of ≤1000 cells/mm3 with a predicted decrease to ≤500 cells/mm3. Fever is defined as a body temperature ≥38.3 Celsius degrees at least once a day with no definite external factor or a body temperature of ≥38 Celsius degrees continued for at least 1 hour.

研究设计

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

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with neutropenic fever who receive therapy for inhibiting or preventing development of neoplasms (abnormal growth of tissue) or stem cell transplantation (stem cell is a cell whose daughter cells may differentiate into other cell types) for hematologic malignancies (cancers that affect blood, bone marrow and lymph nodes)
  • Patients who receive itraconazole intravenous (IV) treatment for more than 7 days

排除标准

  • Childbearing women who are pregnant or likely to be pregnant during the study period and men who are neither infertile nor willing to refrain from sexual relations but whose partner does not conduct an effective contraception
  • Fever due to documented fungal infection
  • Hepatic dysfunction
  • Kidney abnormalities
  • Patients who are not eligible for the study participation based on warnings, precautions and contra medications in the package insert of the study drug at the investigator's discretion

研究组 & 干预措施

Itraconazole

干预措施: Itraconazole (Drug)

结局指标

主要结局

Success rate of itraconazole treatment when used for more than 7 days

时间窗: From 7 days to approximately 2 weeks

Treatment success is achieved when neutropenia is resolved, ie, when the blood cells count is within the normal reference range.

次要结局

  • Success rate of itraconazole treatment until neutropenia is resolved(Approximately 2 weeks)
  • Drop out rate due to the lack of efficacy of itraconazole treatment(Approximately 2 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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