CTRI/2014/03/004485已完成4 期
A prospective observational study of real world treatment outcomes in patients receiving colistimethate sodium
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- Cipla Ltd
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Pms
入排标准
入选标准
- •1.Greater than 18 years
- •2.A written informed consent
- •3.Patients suitable for treatment with colistimethate sodium, including immuno-compromised patients
排除标准
- •1.Patients with hypersensitivity to colistimethate sodium or any exipients of its formulation.
- •2.Patients with Myasthenia gravis.
研究者
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