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临床试验/ISRCTN18011364
ISRCTN18011364已完成不适用

Vaginal misoprostol for first trimester termination of pregnancy prior to 9 weeks of gestatio

Hong Kong Health Services Research Fund (Hong Kong)0 个研究点目标入组 80 人开始时间: 2002年10月14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
80

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. The duration of menstrual delay is less than 49 days
  • 2. The size of the uterus on pelvic examination is compatible with the estimated duration of pregnancy
  • 3. A positive pregnancy test
  • 4. There is no history of significant medical illness
  • 5. Age greater than 16 years old
  • 6. Requests legal termination of pregnancy

排除标准

  • 1. History or evidence of disorders that represent a contraindication to the use of misoprostol (mitral stenosis, glaucoma, sickle cell anaemia, diastolic pressure >100 mm Hg, bronchial asthma)
  • 2. History or evidence of thrombo-embolism, severe or recurrent liver disease or pruritus of pregnancy
  • 3. Presence of intrauterine contraceptive device (IUCD) in utero
  • 4. Suspect or proven ectopic pregnancy
  • 5. Heavy smoker (smoking >10 cigarettes daily in the past 2 years) or had another risk factor for cardiovascular disease

研究者

发起方
Hong Kong Health Services Research Fund (Hong Kong)

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