About this trial
A randomized clinical trial to assess the efficiency of acetylsalicylic acid (aspirin) 150 mg/day started before 20 weeks of gestation in the prevention on maternal and fœtal complications in pregnant women with chronic hypertension.
Eligibility criteria
Qualifiers
Pregnant patient between 10 and 19 weeks of gestation + 6 days
Chronic hypertension, whether treated or not, know before pregnancy or diagnosed before randomization
Singleton pregnancy
Signed the written informed consent
Disqualifiers
---Medical history requiring anticoagulation (antiphospholipid syndrome, deep vein thromboembolic disease, pulmonary embolism, atherothrombosis, patient with mechanical heart valves),
Patient receiving aspirin for another indication outside pregnancy,
Patient with significant proteinuria (> 300mg/24 hours or a proteinuria/creatininuria ratio ≥ 30mg/mmol),
Active bleeding,
Trial design
Treatments tested in this trial
- Aspirin 150 mg
- Placebo