About this trial
This study's primary purpose is to determine the relationship between aspirin metabolism and markers of metabolic dysfunction among patients at risk for preeclampsia.
Eligibility criteria
Qualifiers
Recommended aspirin for pre-eclampsia prevention by OB/GYN or MFM specialist based on ACOG and USPSTF guidelines (1 high risk factor, 2+ moderate risk factors)
Willingness to adhere to aspirin therapy
Willingness to undergo 2h OGTT for serum and urine collection in addition to survey collection, indirect calorimetry, body composition measures, neonatal measures, etc.
Gestational age at enrollment <16 weeks
Disqualifiers
Type 2 Diabetes Mellitus
Type 1 Diabetes Mellitus
Current gestational diabetes mellitus
Current/active platelet disorder or bleeding diathesis (thrombocytopenia of any etiology, idiopathic thrombocytopenic purpura/ITP, thrombotic thrombocytopenic purpura/TTP, von Willebrand disease, etc.)
Trial design
Treatments tested in this trial
- Not listed