EUCTR2008-007973-19-DE进行中（未招募）不适用
Pharmacologic optimization of voriconazole - a prospective clustered group-randomized cross-over trial of therapeutic drug monitoring
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 192
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1) are at least 18 years of age
- •2) have received chemotherapy for haematological malignancies or have received a hematopoietic stem cell transplant
- •3) proven, probable or possible invasive fungal disease according to the EORTC/MSG criteria
- •4) treatment with voriconazole < 3 days, dosed according to product brochure
- •5) written informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 150
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •1) allergic to voriconazole or its excipients
- •2) age below 18 years
- •3) women who are pregnant or who are of child-bearing potential and sexually active who are not practicing an effective method of birth control
- •4) women who are nursing
研究者
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