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NCT05521776Recruiting

Impact of First-trimester Preeclampsia Screening on Perinatal and Maternal Morbidity (RANSPRE)

Impact of First-trimester Preeclampsia Screening on Perinatal and Maternal Morbidity : a Multicenter Randomized Trial

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

The purpose of this study is to determine whether first-trimester screening for preeclampsia based on the FMF algorithm (a combination of maternal clinical, sonographic and biochemical parameters), improves maternal or perinatal health.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
14500 (estimated)
First submitted
7 Jul 2022
Start date
6 Mar 2023
Primary completion date
Aug 2026
Lead sponsor
Assistance Publique - Hôpitaux de Paris
NCT number
NCT05521776

What you commit to

  • Study type: Interventional
  • Planned participants: 14500
  • From 6 Mar 2023 to the primary completion date, Aug 2026
  • 22 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of PE in a previous pregnancy

Other illness

  • Contra-indication to aspirin (bleeding disorders such as von Willebrand's disease, active peptic ulceration, hypersensitivity to aspirin, active peptic ulceration, NSAID-exacerbated respiratory disease, severe liver or heart dysfunction)

Age

  • Gestational age \<11 WG or \>14 WG
  • Age \<18 years

Other

  • Known ectopic pregnancy
  • Known non-ongoing pregnancy
  • Known multiple pregnancy
  • Pregnancies complicated by major fetal abnormality identified at the first-trimester ultrasound if performed before randomization
  • Absence of health insurance
  • Women taking low-dose aspirin regularly and started before pregnancy (except ART indication)
  • Poor understanding of the French language

Who the study is looking for

  • Pregnancy between 11 and 14 WG
  • Age ≥18 years
  • Affiliated to or beneficiary of a health insurance system (including AME)
  • Signed informed consent

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (22)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Angers
Coordinator of this site? Confirm its status
AngersFranceRecruiting
CHU de Bordeaux
Coordinator of this site? Confirm its status
BordeauxFranceRecruiting
Hôpital Femme Mère Enfant
Coordinator of this site? Confirm its status
BronFranceRecruiting
Hopital Antoine Beclere
Coordinator of this site? Confirm its status
ClamartFranceRecruiting
CHU Estaing
Coordinator of this site? Confirm its status
Clermont-FerrandFranceRecruiting
Hôpital Intercommunal Créteil
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CréteilFranceRecruiting
Chu Dijon Bourgogne
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DijonFranceRecruiting
CHU Lille
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LilleFranceRecruiting
Hôpital de la conception et de la Timone
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MarseilleFranceRecruiting
Hôpital Nord
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MarseilleFranceRecruiting
CHRU de Nancy
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NancyFranceRecruiting
Hôpital Femme - Maternité
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NantesFranceRecruiting
Hôpital Cochin - Site Port-Royal
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ParisFranceRecruiting
Hôpital Armand-Trousseau
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ParisFranceRecruiting
Hopital Saint Joseph
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ParisFranceRecruiting
CHI de Poissy
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PoissyFranceRecruiting
Hôpital Sud Rennes
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RennesFranceRecruiting
CHU Charles Nicolle
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RouenFranceRecruiting
Hôpital de Hautepierre
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StrasbourgFranceRecruiting
CHU Strasbourg, CMCO Schiltigheim
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StrasbourgFranceRecruiting
Hopital Paule de Viguier
Coordinator of this site? Confirm its status
ToulouseFranceRecruiting
Hopital Bretonneau
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ToursFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.