ISRCTN09944151已完成不适用
Second trimester termination of pregnancy, outcome after one or two day mifepristone-misoprostol interval: a randomised controlled trial
Helsinki University Hospital (Finland)0 个研究点目标入组 200 人开始时间: 2009年1月16日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 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
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Age over 18 years
- •2. Duration of pregnancy (as verified by ultrasonography) between 12 weeks (12+1) up to 24 weeks (24+0) and approval for termination from the Finnish National Authority for Medico-legal Affairs (TEO)
- •3. Singleton, live pregnancy
- •4. Voluntary participation and signed approval to the study
- •5. No intrauterine device (IUD) in utero at the time of abortion
排除标准
- •1. Allergy to mifepristone or misoprostol
- •2. Severe, complicated asthma
- •3. An extrauterine pregnancy
- •4. No common language with the investigators
- •5. A coronary disease or high risk factors for it
- •6. HIV or hepatitis (a smaller group having blood samples taken)
研究者
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