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NCT05625724RecruitingPhase 3

Aspirin for the Prevention of Preeclampsia and Pregnancy Outcomes After Assisted Reproductive Technology

Aspirin for the Prevention of Preeclampsia and Pregnancy Outcomes in Nulliparous Women After Assisted Reproductive Technology. APPART

Source: ClinicalTrials.gov · Last updated 7 May 2026

Brief summary (registry, in English)

This study seeks to validate the hypothesis that nulliparous pregnant women after Assisted Reproductive Technology (ART) are at high risk of preeclampsia and perinatal complications and represent a subgroup for which aspirin prophylaxis during pregnancy may be effective in the prevention of preterm preeclampsia and other perinatal adverse outcomes.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
1164 (estimated)
First submitted
14 Nov 2022
Start date
2 Aug 2023
Primary completion date
Aug 2028
Lead sponsor
University Hospital, Toulouse
NCT number
NCT05625724

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 1164
  • From 2 Aug 2023 to the primary completion date, Aug 2028
  • 21 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

  • Regular treatment with aspirin (including antiphospholipid syndrome)

Other illness

  • Aspirin contraindications (allergy, von Willebrand disease, peptic ulceration, hemophilia)

Other

  • Major fetal abnormality
  • Women protected by law.
  • Women included in another interventional study.

Who the study is looking for

  • Nulliparous women aged 18 years or more
  • Pregnancy following ART, including in vitro fertilization (IVF), intracytoplasmic sperm injection (ICSI), oocyte donation or intrauterine insemination with sperm donor
  • Singleton pregnancy
  • Evolutive pregnancy between 9 and 14 weeks of gestation
  • Women affiliated to a French Social Security Insurance or equivalent social protection
  • Written informed consent

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

Full criteria on ClinicalTrials.gov

Sites (21)

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

SiteCityCountrySite status
CHU Angers
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AngersFranceRecruiting
CHU Bordeaux
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BordeauxFranceRecruiting
CHU Clermont-Ferrand
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Clermont-FerrandFranceRecruiting
Chu Dijon Bourgogne
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DijonFranceRecruiting
CHU Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting
HCL - Groupement Hospitalier Est, Hôpital Femme Mère Enfant
Coordinator of this site? Confirm its status
LyonFranceRecruiting
AP-HM Hôpital Nord
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MarseilleFranceRecruiting
AP-HM Hôpital de la Conception
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MarseilleFranceRecruiting
CHU Montpellier
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MontpellierFranceRecruiting
CHRU Nancy
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NancyFranceRecruiting
CHU Nantes
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NantesFranceRecruiting
CHU Nîmes
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NîmesFranceRecruiting
Hôpital Armand-Trousseau
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ParisFranceNot yet recruiting
Groupe hospitalier St Joseph
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ParisFranceRecruiting
Hôpital Cochin
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ParisFranceRecruiting
CHI Poissy-Saint-Germain en Laye
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PoissyFranceRecruiting
CHU Poitiers
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PoitiersFranceNot yet recruiting
CHU Rennes
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RennesFranceRecruiting
CHU Saint Etienne Hôpital Nord
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Saint-EtienneFranceRecruiting
CHU Strasbourg
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StrasbourgFranceRecruiting
CHU Toulouse
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ToulouseFranceRecruiting

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