ISRCTN97410750
Completed
未知
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 sites1,200 target enrollmentMarch 6, 2009
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Calthorpe Clinic (UK)
- Enrollment
- 1200
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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