跳至主要内容
临床试验/NCT01020461
NCT01020461终止4 期

Evaluation of Accuvein for Blood Sampling and for Intravenous Catheter Placement in Adult Patients

Hopital Foch1 个研究点 分布在 1 个国家目标入组 522 人开始时间: 2010年1月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
终止
发起方
Hopital Foch
入组人数
522
试验地点
1
主要终点
Time to successful blood sampling or to successful placement of IV catheter

研究概览

简要总结

The objective of this study is to evaluate the effectiveness of Accuvein to facilitate venous blood sampling and placement of peripheral intravenous catheters in adults. This clinical protocol is designed to determine whether using Accuvein increases the ease and efficiency of venous cannulation (as perceived by the operator), decreases the time to effective cannulation, decreases the number of sticks, and decreases the patient's perception of the pain.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •adults requiring a venous blood sampling or the placement of a venous peripheral catheter

排除标准

  • 未提供

研究组 & 干预措施

Venous blood sampling

Experimental

To use Accuvein to improve the effectiveness of venous blood sampling

干预措施: Accuvein (Device)

Peripheral IV catheter placement

Experimental

To use Accuvein to improve the effectiveness of placing peripheral IV catheter

干预措施: Accuvein (Device)

结局指标

主要结局

Time to successful blood sampling or to successful placement of IV catheter

时间窗: one hour

次要结局

  • Number of attempts required(Immediately after attempts)
  • Pain(Immediately after attempts)
  • Increases in the ease and efficiency of venous cannulation perceived by the operator)(Immediately after attempts)

研究者

发起方
Hopital Foch
申办方类型
Other
责任方
Sponsor

研究点 (1)

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