Status:
COMPLETED
Routine Follow-up Versus Self-assessment in Medical Abortion
Lead Sponsor:
Karolinska Institutet
Collaborating Sponsors:
Ullevaal University Hospital
University of Helsinki
Conditions:
Medical Abortion
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The main objective of the study is to optimize the routines for follow-up after medical abortion in order to give women more autonomy by reducing the number of consultations involved and to reduce the...
Eligibility Criteria
Inclusion
- women requesting termination of pregnancy by means of mifepristone followed by home administration of misoprostol at \< /=63 days of gestation, with no contraindication to medical abortion and self administration of misoprostol at home, and who have given their informed consent will be eligible for study recruitment.
Exclusion
- women who do not wish to participate
- women who do not want home administration of misoprostol
- women who are unable to communicate in Swedish, Norwegian, English, Finnish or German and women with symptoms and signs of ectopic pregnancy
- minors (i.e. women \< 18 years of age) will not be enrolled for the study.
- women seeking termination of pregnancy with no sign of a visible intrauterine pregnancy (i.e. visible intrauterine yolk sac).
Key Trial Info
Start Date :
September 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2013
Estimated Enrollment :
929 Patients enrolled
Trial Details
Trial ID
NCT01487213
Start Date
September 1 2011
End Date
July 1 2013
Last Update
August 7 2013
Active Locations (4)
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1
GynMed Clinic
Vienna, Austria
2
Dept. Obstetrics and Gynaecology,Helsinki University Central Hospital
Helsinki, Finland
3
Faculty of Medicine, University of Oslo and Dept. of Gynaecology,
Oslo, Norway
4
Dept of Obstetrics and Gynecology, Karolinska University Hospital
Stockholm, Sweden, SE17176