跳至主要内容
临床试验/NCT01543009
NCT01543009暂停1 期

Use of Local Warming in Children to Facilitate Venipuncture. A Randomized Controlled Trial.

University of Florence1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2012年3月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
暂停
入组人数
72
试验地点
1
主要终点
rate of success of peripheral venous cannulation at the first attempt

研究概览

简要总结

The aim of this study is to determine if local application of heat increases the probability of insertion of peripheral venous catheter at the first attempt, reduces the time needed to obtain cannulation and maintains the analgesic effect of Emla in children undergoing peripheral venous cannulation and previously treated with local analgesia with Emla.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
8 Years 至 13 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •age between 8 and 13 years
  • •Intravenous drug therapy prescribed by a physician
  • •no allergy to lidocaine
  • •no local skin disease
  • •absence of burns scars
  • •child and his/her family are native speaker of Italian
  • •BMI not lower than 10° centile for sex and age according to the CDC standards

排除标准

  • •age of child not included in the age range established for the study
  • •Intravenous drug therapy not needed
  • •Presence of an allergy to lidocaine products
  • •Skin disease
  • •Presence of burns scars
  • •The child or his/her family are not native speaker Italian
  • •BMI lower than 10° centile according to the CDC standards

研究组 & 干预措施

Emla + no additional intervention

No Intervention

Children in this arm will receive standard preparation of the venipuncture site (local analgesia with Emla) without warming

Emla + Local Warming

Experimental

Children in this arm will receive standard preparation of the venipuncture site (local analgesia with Emla) plus warming with a heating pad at 40°C for 5 minutes

干预措施: Emla + Local Warming (Other)

结局指标

主要结局

rate of success of peripheral venous cannulation at the first attempt

时间窗: The outcome is observed and recorded immediatly after the venous cannulation. No follow up is required

次要结局

  • pain perceived by the child undergone to the cannulation(The outcome is observed and recorded immediatly after the venous cannulation. No follow up is required)
  • Difficulty in performing cannulation perceived by Nurse(The outcome is observed and recorded immediatly after the venous cannulation. No follow up is required)
  • Time needed to obtain cannulation(From positioning tourniquet to completion of cannulation. No follow up is required)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Filippo Festini

Professor of Nursing

University of Florence

研究点 (1)

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