TCTR20180802002招募中4 期
Efficacy of pain relief during first trimester surgical abortion : randomized clinical trial compared intravenous sedation, paracervical block and lidocaine spray added to paracervical block
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 165
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
- 15 Years 至 45 Years（—）
- 性别
- Female
入选标准
- •pregnant woman with gestational age below 14 weeks who diagnosed incomplete abortion
排除标准
- •- allergy to meperidine or lidocaine
- •- septic abortion
- •- unstable vital signs
- •- patients who can not communicate and unconscious
研究者
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