NCT01212601已完成不适用
A Multicenter, Observational, Non-interventional Registry Designed to Collect Clinical Data in Chinese Patients Who Have Received CUBICIN® Treatment Under Condition of Actual Usage in Clinical Practice
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AstraZeneca
- 入组人数
- 203
- 试验地点
- 1
- 主要终点
- AEs of CUBICIN therapy
研究概览
简要总结
This is a Multicenter, observational, non-interventional registry designed to collect clinical data in Chinese patients who have received CUBICIN treatment under condition of actual usage in clinical practice.
详细描述
MC MD
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient has received CUBICIN treatment, decided by treating physician
- •A patient who is considered as ethnic Chinese
- •Provision of subject informed consent
排除标准
- •A patient record will not be eligible for the registry database if the patient received CUBICIN as part of a controlled clinical study for the current infection episode.
结局指标
主要结局
AEs of CUBICIN therapy
时间窗: 2 weeks
clinical response of CUBICIN therapy at each available time point
时间窗: 2 weeks
次要结局
- CPK level monitoring and results(2 weeks)
- treatment duration(2 weeks)
- Time to clinical response(2 weeks)
研究者
研究点 (1)
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