NL-OMON43049招募中不适用
Defining the optimal dose for continuous flucloxacillin infusion using pharmacokinetic modelling ;The FLUCON-study - Flucon
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
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
- 18 至 99（—）
入选标准
- •Part A;In order to be eligible to participate in this study, a subject must meet;all of the following criteria:;- The patient is at least 18 years of age;- The patient has started with intravenous flucloxacillin as indicated by;their physician;At least 10 of the 30 patients are treated with flucloxacillin for a bacteriemia;Part B;In order to be eligible to participate in this study, a subject must meet;all of the following criteria:;- The patient is at least 18 years of age;- The patient has an indication for the treatment of flucloxacillin with;continuous infusion as indicated by their physician
排除标准
- •Part A and B;A potential subject who meets any of the following criteria will be;excluded from participation in this study because of the altered;pharmacokinetics:;- The patient who is admitted to the intensive care unit;- Pregnant women
研究者
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