A randomised controlled trial on Efficacy of mifepristone followed by 6-8 hours versus 24 hours vaginal misoprostol in Early Medical Abortions (< 63 days gestation)

Calthorpe Clinic (UK)0 个研究点目标入组 1,200 人开始时间: 2009年3月6日最近更新: 2017年7月3日

试验速览

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•1. Ability to give informed written consent
•2. Women who are 18 years and older
•3. Requesting abortion and eligible for legal termination of pregnancy
•4. Duration of pregnancy not more than 63 days (counted from the first day of the last menstrual period) in a normal 28-day cycle or verified by ultrasound
•5. The pregnancy is single and intrauterine (single sac)
•6. Agree to be able to be contacted by telephone (i.e. mobile telephone)
•7. Women with limited understanding of English will be included only in the quantitative study where interpreters are available

•1. Any indication of serious past or present ill health will be considered a contraindication for recruitment to the study
•2. Suspicion of any pathology of pregnancy (e.g. molar, non-viable pregnancy, threatened abortion)
•3. Current participation in a drug-related trial
•4. Non-English-speaking women for the qualitative study
•5. Women under the age of 18 years

发起方

Calthorpe Clinic (UK)