ACTRN12609000796280尚未招募2 期
A comparison of a vapocoolant spray (Pain Ease) with Amethocaine Gel (AnGel) to reduce the pain associated with intravenous(IV) cannulation in children.
Dr Benjamin D'Souza0 个研究点目标入组 280 人开始时间: 2009年9月15日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 280
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
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 6 Years 至 18 Years（—）
- 性别
- All
入选标准
- •Children between 6 and 18 yrs of age, presenting to the pediatric emergency department(PED) and requiring IV cannulation
排除标准
- •Patients requiring urgent vascular access
- •Patients with impaired consciousness, a history of psychiatric illness or with developmental delay
- •Use of opioid analgesics or sedating agents within 4 hours of enrollment
- •Patients with pain score of greater than 6 (Pain Scale 0-10), i.e. requiring urgent analgesia
- •In patients with Diabetes Mellitus or patients with Cold hypersensitivity as Pain Ease is specifically contraindicated in these groups.
- •Sensitivity or previous adverse reactions to halogenated hydrocarbons or amethocaine
- •Non English speaking families
- •Those unable to understand the study protocol or the Visual Analog scale
研究者
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