NL-OMON50150已完成4 期
Ciprofloxacin pharmacokinetics after IV and oral administration in cachectic elderly patients - CIPCEP
Tergooiziekenhuizen0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 25
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Treated witch ciprofloxacin as a part of routine clinical care
- •- >75 years of age
- •- At least one of the following:
- •o Unintended weight loss of >10% of total body weight in the previous 12 months
- •o weight <60kg and BMI<21
- •o BMI <21 and a positive MUST score for malnutrition
- •- Participant is able and willing to sign the Informed consent before screening
- •evaluations.
排除标准
- •- Subjects may not be critically ill, i.e. not be admitted to the ICU
研究者
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