ACTRN12615000667516已完成3 期
Randomised controlled trial of tissue adhesive, integrated securement products or external stabilisation devices versus standard care (bordered polyurethane) dressings to prevent central venous access device failure in intensive care patients with non-tunnelled, percutaneous central venous access devices: the CASCADE ICU trial
Associate Professor Marion Mitchell0 个研究点目标入组 120 人开始时间: 2015年6月26日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 120
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
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 16 Years 至 o limit（—）
- 性别
- All
入选标准
- •1. Informed written consent
- •2. Non-tunnelled percutaneous CVAD to be inserted in ICU for clinical care for >24 hours
排除标准
- •1. Peripherally inserted, tunnelled, dialysis, or pulmonary artery catheters;
- •2. Current bloodstream infection;
- •3. CVAD to be inserted through diseased, burned, scarred or hirsute skin;
- •4. Allergy to any study product;
- •5. Previous study enrolment in this admission
研究者
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