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RECRUITING
NCT05625724
PHASE3

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

Sponsor: University Hospital, Toulouse

View on ClinicalTrials.gov

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.

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

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

1164

Start Date

2023-08-02

Completion Date

2026-05

Last Updated

2024-01-22

Healthy Volunteers

No

Interventions

DRUG

Aspirin

Experimental drug administrated orally

DRUG

Placebo

Treatment for the control group

Locations (21)

CHU Angers

Angers, France

CHU Bordeaux

Bordeaux, France

CHU Clermont-Ferrand

Clermont-Ferrand, France

CHU Dijon-Bourgogne

Dijon, France

CHU Lille

Lille, France

HCL - Groupement Hospitalier Est, Hôpital Femme Mère Enfant

Lyon, France

AP-HM Hôpital de la Conception

Marseille, France

AP-HM Hôpital Nord

Marseille, France

CHU Montpellier

Montpellier, France

CHRU Nancy

Nancy, France

CHU Nantes

Nantes, France

CHU Nîmes

Nîmes, France

Groupe hospitalier St Joseph

Paris, France

Hôpital Armand - Trousseau

Paris, France

Hôpital Cochin

Paris, France

CHI Poissy Saint Germain en Laye

Poissy, France

CHU Poitiers

Poitiers, France

CHU Rennes

Rennes, France

CHU Saint Etienne, Hôpital Nord

Saint-Etienne, France

CHU Strasbourg

Strasbourg, France

CHU Toulouse

Toulouse, France