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Medical abortion at 10-20 weeks

Not Applicable
Completed
Conditions
Pregnancy of 64-140 days duration
Pregnancy and Childbirth
Registration Number
ISRCTN49711898
Lead Sponsor
Concept Foundation (Switzerland)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
670
Inclusion Criteria

1. Good general health
2. Older than the age for legal consent
3. Requesting and eligible for legal termination of pregnancy
4. Duration of pregnancy 64-140 days on Day 1 (mifepristone administration), verified by ultrasound

Exclusion Criteria

1. No contra-indications towards mifepristone and misoprostol
2. No serious present or past ill health
3. Molar or extrauterine pregnancy or threathend abortion, >1 low segment C-section

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Efficacy (expulsion of pregnancy) at 24 h
Secondary Outcome Measures
NameTimeMethod
<br> 1. Induction-to-abortion interval: This is the time interval from the administration of the first dose of misoprostol until expulsion of the products of conception<br> 2. Possible side-effects: Side effects are recorded during the whole study, from the administration of mifepristone until the follow-up visit, or beyond, if needed<br> 3. Women's perceptions: Women's perception of the method are recorded at an interview during the follow-up visit about two weeks after treatment<br>
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