NL-OMON35993已完成4 期
A randomised clinical trial on the effectiveness of Emla and Rapydan for prevention of vena punction-induced pain in children. - Pain perception after vena punction.
Isala Klinieken0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 2 至 17（—）
入选标准
- •Age 3 - 18
排除标准
- •Allergy for the contents of the plaster
研究者
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