About this trial
Title: A prospective multicentric interventional randomized controlled trial to assess the effect of low dose acetylsalicylic acid as a preventive treatment of pre-eclampsia in pregnant women who underwent frozen embryo transfer
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Healthy women from [18 - 43] years-old, planned for a frozen embryo transfer, with natural and modified natural or HRT cycle
Who have given their informed consent
Who have a confirmed pregnancy at week 6 of amenorrhea.
Disqualifiers
Women presenting one risk factor for preeclampsia: multiple pregnancy, history of preeclampsia, BMI > 30, lupus syndrome, preexistent proteinuria, non-treated chronic high blood pressure (>140/90), antiphospholipid antibody syndrome, diabetes (fasting blood sugar >126mg/dl)
Contraindication to acetylsalicylic acid (at risk of active hemorrhage (like hemophilia, …); at risk of or who have a gastro-duodenal ulcer; at risk or how have a terminal renal or hepatic in-sufficiency (only if acetylsalicylic acid is given at high dose)
Already treated with acetylsalicylic acid
Treatment with anticoagulants or non-steroid anti-inflammatory drugs
Trial design
Parallel
Treatments tested in this trial
Acetylsalicylic acid
Drug160mg once a day
Treatment groups
Trial outcomes
Primary outcomes
Mean number of women suffering from pre-eclampsia in the treated and not treated groups.
Sponsors and contacts
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Centre Hospitalier Universitaire de Liege
Lead sponsor
Centre Hospitalier Régional de la Citadelle
Sponsor institution