Does Progesterone Prevent Very Preterm Delivery in Twin Pregnancies?
Preterm Delivery

About this trial
This is an interventional prevention trial for Preterm Delivery focused on measuring Preterm delivery, Prevention, Twins, Progesterone
Eligibility Criteria
Inclusion Criteria: Twin pregnancy Informed consent 18-23 weeks' gestation Participants must be fluent in the language spoken in the respective centres Exclusion Criteria: Age < 18 years Known allergy to progesterone or peanuts Active thromboembolic disorders or a history of hormone-associated thromboembolic disorders Rupture of membranes at the time of inclusion Monoamniotic twins Pregnancies treated for or with signs of twin-to-twin transfusion syndrome at inclusion Multiple pregnancies reduced to twin pregnancies Known significant structural or chromosomal fetal abnormality Chorionicity not assessed before 15 weeks Known or suspected malignancy in genitals or breasts Known liver disease
Sites / Locations
- Graz University Hospital
- Innsbruck University Hospital
- Klagenfurt Hospital
- Vienna University Hospital
- Aalborg Hospital
- Skejby Hospital
- Rigshospitalet
- Glostrup Hospital
- Gentofte Hospital
- Herlev Hospital
- Hilleroed Hospital
- Holbaek Hospital
- Hvidovre Hospital
- Odense University Hospital
- Roskilde Hospital
- Soenderborg Hospital
- Viborg Hospital
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Active Comparator
Placebo
Progesterone