RecruitingNot applicableNCT05521776
Impact of First-trimester Preeclampsia Screening on Perinatal and Maternal Morbidity (RANSPRE)
Studying Preeclampsia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Assistance Publique - Hôpitaux de Paris
- Principal Investigator
- Catherine DENEUX, MD, PhDInstitut National de la Santé Et de la Recherche Médicale, France
- Intervention
- First-trimester preeclampsia screening (FMF triple test)(procedure)
- Enrollment
- 14500 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2023 – 2027
Study locations (22)
- CHU Angers, Angers, France
- CHU de Bordeaux, Bordeaux, France
- Hôpital Femme Mère Enfant, Bron, France
- Hôpital Antoine Béclère, Clamart, France
- CHU Estaing, Clermont-Ferrand, France
- Hôpital Intercommunal Créteil, Créteil, France
- CHU Dijon Bourgogne, Dijon, France
- CHU Lille, Lille, France
- Hôpital de la conception et de la Timone, Marseille, France
- Hôpital Nord, Marseille, France
- CHRU de Nancy, Nancy, France
- Hôpital Femme - Maternité, Nantes, France
- Hôpital Armand Trousseau, Paris, France
- Hôpital Cochin (site Port-Royal), Paris, France
- Hôpital Saint-Joseph, Paris, France
- +7 more locations on ClinicalTrials.gov
Collaborators
INSERM, Epopé team · URC-CIC Paris Descartes Necker Cochin
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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