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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.
Preeclampsia (PE) affects 2% of pregnancies in France and is an important cause of maternal and perinatal mortality and morbidity. Aspirin is currently the only prophylactic therapy for PE in high-risk women when initiated before 16 weeks of gestation and at a daily dose of 100-160 mg, with a reduction in the incidence of preterm preeclampsia of 60-70% in recent meta-analysis. Latest data also demonstrate a potential beneficial effect of aspirin on spontaneous preterm birth. A major challenge in modern obstetrics is early identification of pregnant women at high-risk of PE who could benefit from aspirin treatment. In France, the College National des Gynécologues et Obstétriciens Français and the Société Française d'HyperTension Artérielle have restrictive recommendation of aspirin to be prescribed only to women with a history of PE or vascular intra-uterine growth restriction, thus leaving out all nulliparous women (including those with multiple risk factors). Other countries (USA, United Kingdom (UK), Canada) have much broader recommendations with aspirin prescription for patients with one high or 2 moderate risk factors, but exposing nearly 30% of pregnant women to aspirin (leading to unnecessary exposure to treatment). The Fetal Medicine Foundation provides a screening test combining clinical parameters, uterine artery Doppler, and biomarkers; but this strategy has high false-positive rate and the reproducibility needs to be confirmed in clinical practice.
It seems necessary to be able to better target women at risk, especially in nulliparous women. Nulliparity and assisted reproductive technology (ART) are independent risk factors for PE. Currently the proportion of pregnancy after ART in France is roughly 6.9% and is rising. Nulliparous ART pregnant women have a higher risk of PE and preterm birth. Indeed, they commonly cumulate risk factors including age>35years in association with nulliparity and ART. The rate of PE in this population can rise up to 10%.
Our hypothesis is that nulliparous pregnant women after 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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Aspirin | Experimental | Low-dose Aspirin: 150mg, daily, oral route, at bedtime, initiated between 9 and 14 weeks of gestation, until 35 (+6) weeks of gestation, or in the event of earlier delivery, until the onset of labor. |
|
| Control | Placebo Comparator | Matching placebo administrated daily, oral route, at bedtime, initiated between 9 and 14 weeks of gestation, until 35 (+6) weeks of gestation, or in the event of earlier delivery, until the onset of labor. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Aspirin | Drug | Experimental drug administrated orally |
| |
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo in the prevention of preterm (<37 weeks of gestation) preeclampsia | Occurrence of preterm (<37 weeks of gestation) preeclampsia (binary variable yes/no) | Up to 9 months |
| Measure | Description | Time Frame |
|---|---|---|
| Compare the effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo on spontaneous and total preterm birth <34 weeks of gestation | Occurrence of spontaneous and total preterm birth (defined by delivery at <34 weeks of gestation) | Up to 8 months |
| Compare the effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo on spontaneous and total preterm birth <37 weeks of gestation |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Paul GUERBY, MD | Contact | 5 67 77 12 33 | guerby.p@chu-toulouse.fr | |
| Delphine DUCHANOIS, Midwife | Contact | 5 67 77 12 33 | +33 | duchanois.d@chu-toulouse.fr |
| Name | Affiliation | Role |
|---|---|---|
| Christophe VAYSSIERE, MD | University Hospital, Toulouse | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU Angers | Recruiting | Angers | France |
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| Drug |
Treatment for the control group |
|
Occurrence of spontaneous and total preterm birth (defined by delivery at <37weeks of gestation) |
| Up to 9 months |
| Compare the effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo on occurrence of preeclampsia <34 weeks of gestation, term preeclampsia (≥ 37 weeks of gestation) | Occurrence of term (≥37 weeks) preeclampsia | Up to 8 months |
| Compare the effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo on occurrence of cesarean delivery | Occurrence of cesarean delivery | Up to 9 months |
| Compare the effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo on occurrence of postpartum hemorrhage (>500ml) | Occurrence of postpartum hemorrhage (>500ml) | Up to 9 months |
| Compare the effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo on occurrence of placental abruption | Occurrence of placental abruption | Up to 9 months |
| Compare the effect of aspirin 150mg daily initiated between 9 and 14 weeks of gestation versus placebo on neonatal adverse outcome. | Occurrence of neonatal adverse outcomes: still birth, neonatal death, neonatal complications | Up to 9 months |
| CHU Bordeaux | Recruiting | Bordeaux | France |
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| CHU Clermont-Ferrand | Recruiting | Clermont-Ferrand | France |
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| CHU Dijon-Bourgogne | Recruiting | Dijon | France |
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| CHU Lille | Recruiting | Lille | France |
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| HCL - Groupement Hospitalier Est, Hôpital Femme Mère Enfant | Recruiting | Lyon | France |
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| AP-HM Hôpital de la Conception | Recruiting | Marseille | France |
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| AP-HM Hôpital Nord | Recruiting | Marseille | France |
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| CHU Montpellier | Recruiting | Montpellier | France |
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| CHRU Nancy | Recruiting | Nancy | France |
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| CHU Nantes | Recruiting | Nantes | France |
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| CHU Nîmes | Recruiting | Nîmes | France |
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| Groupe hospitalier St Joseph | Recruiting | Paris | France |
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| Hôpital Armand - Trousseau | Not yet recruiting | Paris | France |
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| Hôpital Cochin | Recruiting | Paris | France |
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| CHI Poissy Saint Germain en Laye | Recruiting | Poissy | France |
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| CHU Poitiers | Not yet recruiting | Poitiers | France |
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| CHU Rennes | Recruiting | Rennes | France |
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| CHU Saint Etienne, Hôpital Nord | Recruiting | Saint-Etienne | France |
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| CHU Strasbourg | Recruiting | Strasbourg | France |
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| CHU Toulouse | Recruiting | Toulouse | France |
|
| ID | Term |
|---|---|
| D011225 | Pre-Eclampsia |
| ID | Term |
|---|---|
| D046110 | Hypertension, Pregnancy-Induced |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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| ID | Term |
|---|---|
| D001241 | Aspirin |
| ID | Term |
|---|---|
| D012459 | Salicylates |
| D062385 | Hydroxybenzoates |
| D010636 | Phenols |
| D001555 | Benzene Derivatives |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
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