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NCT05625724
Aspirin for the Prevention of Preeclampsia and Pregnancy Outcomes After Assisted Reproductive Technology
Conditions: ART, Pre-Eclampsia
Sex: Female
Ages: 18 Years – N/A
Phase: PHASE3
Enrollment: 1164
Sponsor: University Hospital, Toulouse
Location: France
Summary
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.
Eligibility Criteria
Inclusion Criteria:Nulliparous women aged 18 years or morePregnancy following ART, including in vitro fertilization (IVF), intracytoplasmic sperm injection (ICSI), oocyte donation or intrauterine insemination with sperm donorSingleton pregnancyEvolutive pregnancy between 9 and 14 weeks of gestationWomen affiliated to a French Social Security Insurance or equivalent social protectionWritten informed consentExclusion Criteria:Major fetal abnormalityRegular treatment with aspirin (including antiphospholipid syndrome)Aspirin contraindications (allergy, von Willebrand disease, peptic ulceration, hemophilia)Women protected by law.Women included in another interventional study.
Source: ClinicalTrials.gov (NCT05625724). StuddyBuddy aggregates publicly available trial information.