DRKS00024211招募中不适用
Comparison of uncoated central venous catheters with and without transient coating as product protection with regard to biofilm formation - CutSep
Solvamed GmbH0 个研究点目标入组 852 人开始时间: 2021年2月18日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 852
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •All patients should be included in the study, which:
- •- be supplied with uncoated central venous catheters
- •- have at least a catheter time of 60 hours
- •- have been given their consent and have understood the consent form
- •- are over 18 years old
排除标准
- •Patients will not be admitted to the clinical trial if any of the following criteria are available:
- •- Catheter lying time less than 60 hours
- •- in front of lying the catheter, there are already positive blood culture evidence on the side of the clinic
- •- The absence of a signed declaration of consent
- •- Pregnant or breastfeeding women
- •- Patients after catheter change
研究者
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