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临床试验/ACTRN12614001329651
ACTRN12614001329651已完成未知

Randomised controlled trial of tissue adhesive, combined securement and dressing product or external stabilisation devices versus standard care (bordered polyurethane) dressings to prevent central venous access device failure in paediatric intensive care patients with percutaneous central venous access devices: the CASCADE Junior PICU trial

Griffith University0 个研究点目标入组 80 人开始时间: 2014年12月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
80

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
o limit 至 16 Years(—)
性别
All

入选标准

  • *Patient requires the insertion of a percutaneous CVAD for >24 hours;
  • *Will remain in admitted to the RCH/LCCH for >24 hours;
  • * Less than 16 years of age; and
  • *Parent or legal guardian, and child if developmentally appropriate, gives informed consent.

排除标准

  • *Tunnelled, peripherally inserted, dialysis, or implanted CVADs or pulmonary artery catheters;
  • *Current bloodstream infection;
  • *CVAD to be inserted through diseased, burned or scarred skin;
  • *Allergy to study product; and
  • *Previous study enrolment in this admission to hospital

研究者

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