ACTRN12611001051932已完成未知
Termination of early pregnancy using mifepristone 200mg followed by buccal administration of misoprostol 800mcg – retrospective review of efficacy and safety – Australian Authorised Prescriber Program.
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 13,000
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
- 14 Years 至 50 Years（—）
- 性别
- Female
入选标准
- •Confirmed pregnancy up to 9 weeks gestation.
- •Informed consent.
- •No contraindications.
- •Must meet legal requirements for termination of pregnancy in the state where the service is provided.
排除标准
- •More than 9 weeks since the last menstrual period (confirmed by ultrasound).
- •Known or suspected ectopic pregnancy.
- •Concomitant administration of anticoagulants or corticosteroids.
- •Adrenal failure, inherited porphyria or a haemorrhagic disorder.
- •Allergy to mifepristone or misoprostol.
- •Intrauterine device insitu
- •Pelvic infection
研究者
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