CTIS2023-509003-32-00招募中1 期
Vancomycin treatment in critically ill adults using model-informed precision dosing tool – prospective low-intervention clinical trial. (ProVanc) - PROVANC1.0
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 56
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 65+（—）
- 性别
- All
入选标准
- •Age =18 years, Admitted to the tertiary intensive care unit in Tartu University Hospital, Patient has indication (assessed by treating doctor) to start intravenous vancomycin treatment
排除标准
- •Patient has been previously enrolled into this study during ongoing hospital record, Patient has previously received vancomycin within last 7 days, Intravenous treatment with vancomycin has begun more than 24h before enrolment to study, The treating physician considers the patient not suitable for the study, There is no intention for vancomycin therapeutic drug monitoring, Continues intravenous vancomycin administration is used
研究者
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