ACTRN12619000798167招募中未知
Effect of a splint and intravenous protection device on peripheral intravenous cannula failure in neonates.
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 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
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
入排标准
- 年龄范围
- Hours 至 28 Days（—）
- 性别
- All
入选标准
- •All neonates admitted to the neonatal unit at Monash Children's Hospital, Clayton with a gestation at birth of more than 35 weeks and birth weight of more than 2500g who require a peripheral intravenous cannula.
- •Only one cannulation per neonate will be included in the study, and this will preferably be the first cannulation.
排除标准
- •Neonates who are expected to require the PIVC for a period of less than 24 hours will be excluded from the study
研究者
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