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临床试验/NCT02504398
NCT02504398Unknown3 期

A Randomized Controlled Trial of Injection Technique for Infant Vaccination

University of Toronto1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2015年7月最近更新:
适应症

试验速览

阶段
3 期
入组人数
120
试验地点
1
主要终点
Infant Behavioural Pain Score

研究概览

简要总结

Vaccine injections are a significant source of pain for infants. Altering the injection speed when administering vaccines may be an effective intervention and is feasible (cost neutral). At present, there are no data regarding impact of injection speed on vaccine injection pain in infants. The aim of this study is to address this knowledge gap and to compare the impact of slow and fast vaccine injection speeds on pain during routine infant vaccinations.

详细描述

To date, there has been no evidence-based guidance regarding the rate at which vaccines should be injected to minimize pain. This has led to a disparity in practice. Some vaccinators favour a slow rate of injection (around 8-10 sec/mL) while others prefer a more rapid rate of injection (around 2-4 sec/mL).The slow injection method leads to a longer needle dwelling time with the increased possibility of the needle moving around and causing pain by damaging muscle tissue. Rapid injection, on the other hand, may lead to a sudden distension of muscle tissue, which itself could be painful. Allowing the muscle sufficient time to distend in order to accommodate the vaccine might minimize pain. This study will address the identified knowledge gap by comparing pain in infants undergoing routine vaccinations with a fast vs. slow injection speed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
2 Months 至 7 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Healthy 2 and 4 month old infants receiving their primary vaccine injections, PediacelTM (0.5mL) and PrevnarTM (0.5mL) (in conjunction with and preceded by oral RotarixTM vaccine) and healthy 6 month old infants receiving their routine vaccine injection, PediacelTM (0.5mL)

排除标准

  • Infants with impaired neurological development; history of seizures; administration of sedatives or narcotics in the preceding 24 hours; parental inability to use study tools; parent vaccine refusal; prior participation in the trial; and refusal to be video recorded

结局指标

主要结局

Infant Behavioural Pain Score

时间窗: up to 1 minute post-vaccinations

Assessed using the Modified Behavioural Pain Scale (0-10) from videotapes of the procedure

次要结局

  • Infant Parent-rated Pain Score(up to 2 minutes)
  • Infant Cry duration(up to 2 minutes)

研究者

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

Anna Taddio

Professor

University of Toronto

研究点 (1)

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