O02.1 O02.0
Conditions
Interventions
Group 1: Patients who undergo medical induction with a mifepristone-misoprostol regimen will be asked to fill out a data sheet daily on the extent of their vaginal bleeding (bleeding in/above normal s
Sponsors
Kepler Universitätsklinikum Linz
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Women with Missed Abortion or Windmole who choose Mifegyne® and Cyprostol® for medical induction - Sonographic = 12+6 pregnancy week or CRL = 60 mm
Exclusion criteria
Exclusion criteria: - Clinically/sonographically Abortus incipiens - Abortus incompletus - Infection - Trophoblastic disease - Multiple pregnancy - Request for appointment at the resident specialist - Insufficient knowledge of German
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of the duration of vaginal bleeding following medical induction on the basis of a data sheet filled in daily by the patients themselves | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of predictive factors for the success of a medical induction (success = no additional measures such as curettage or additional misoprostol doses necessary). The parameters used in the analysis are routinely collected at the beginning of a medical induction of an early pregnancy failure. | — |
Countries
Austria
Contacts
Public ContactSimon-Hermann Enzelsberger
Kepler Universitätsklinikum - Universitätsklinik für Gynäkologie, Geburtshilfe und Gyn. Endokrinologie
Outcome results
None listed