跳至主要内容
临床试验/NCT02674685
NCT02674685已完成不适用

VFEND SPECIAL INVESTIGATION FOR PROPHYLAXIS

Pfizer0 个研究点目标入组 241 人开始时间: 2016年3月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
241
主要终点
Number of Participants With Adverse Drug Reactions

研究概览

简要总结

Examine the safety and effectiveness of Vfend [voriconazole] for prophylaxix use under general clinical practices.

研究设计

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

入排标准

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

入选标准

  • Patients undergoing HSCT (Hematopoietic Stem Cell Transplantation).

排除标准

  • Patients who have been previously enrolled in this study.

结局指标

主要结局

Number of Participants With Adverse Drug Reactions

时间窗: Maximum 3 years

An adverse drug reaction (ADR) was any untoward medical occurrence attributed to VFEND in a participant who received VFEND. A serious ADR was an ADR resulting in any of the following outcomes or deemed significant for any other reason: death; life-threatening experience (immediate risk of dying); initial or prolonged inpatient hospitalization; persistent or significant disability/incapacity; congenital anomaly. Relatedness to VFEND was assessed by the physician.

次要结局

  • Number of Participants With Adverse Drug Reactions Not Expected From the Approved Local Product Document (Unknown Adverse Drug Reactions)(Maximum 3 years)
  • Proportion of Participants Who Developed Invasive Fungal Infections (IFI Rate)(Maximum 3 years)
  • Proportion of Participants With Successful Prophylaxis of Invasive Fungal Infections (Success Rate)(Maximum 3 years)
  • Proportion of Participants With Adverse Drug Reactions by Age(Maximum 3 years)
  • Proportion of Participants Who Developed Invasive Fungal Infections (IFI Rate) by Age(Maximum 3 years)
  • Proportion of Participants With Successful Prophylaxis of Invasive Fungal Infections (Success Rate) by Age(Maximum 3 years)
  • Proportion of Participants With Adverse Drug Reactions by Reason for Use(Maximum 3 years)
  • Proportion of Participants With Adverse Drug Reactions by Long-term Use(Maximum 3 years)
  • Proportion of Participants Who Developed Invasive Fungal Infections (IFI Rate) by Reason for Use(Maximum 3 years)
  • Proportion of Participants With Successful Prophylaxis of Invasive Fungal Infections (Success Rate) by Reason for Use(Maximum 3 years)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

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