A double-blind, randomised, controlled multicentre trial of three misoprostol regimens after pretreatment with mifepristone for termination of early pregnancy
Completed
- Conditions
- AbortionInduced abortionPregnancy and Childbirth
- Registration Number
- ISRCTN81170837
- Lead Sponsor
- DP/UNFPA/WHO/World Bank - Special Programme of Research, Development and Research Training in Human Reproduction (HRP)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 2100
Inclusion Criteria
1. Healthy women
2. Eligible for and requesting medical abortion
3. Prepared to terminate the pregnancy should the treatment fail
Exclusion Criteria
No exclusion criteria
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method