TCTR20201207002已完成4 期
A randomized control trial of Hyoscine N-Butylbromide versus Lidocaine pretreatment for alleviating pain on propofol injection
Faculty of Medicine, Khon Kaen university0 个研究点目标入组 56 人开始时间: 2020年12月7日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 56
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 60 Years（—）
- 性别
- All
入选标准
- •Age 18-60 years old
- •ASA physical status I-II
排除标准
- •Refused to participation
- •Be Allergic to Lidocaine or Hyoscine
- •Prior analgesia, antimuscarinic drug or anti-inflammatory drugs before surgery
- •Chronic pain
- •Diabetes mellitus
- •Unable to communicate/evaluate NRS
- •Contraindication for hyoscine
- •-Gut obstruction or ileus
- •-BPH with urinary retention
- •-Myasthenia gravis
- •-Heart failure
研究者
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