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Nifedipine to Lower Blood Pressure After Preeclampsia Pregnancy

Tests nifedipine to control blood pressure in women after preeclampsia pregnancy.

Plain-language title generated from the registry record
Registry title: Reducing the Risk of Chronic Hypertension and Improving Vascular Function Following Preeclampsia

Key facts

Where
Chicago and Milwaukee, United StatesSee the 2 sites

Where in United States

  • Northwestern UniversityChicago, United StatesTaking people
  • Medical College of WisconsinMilwaukee, United StatesTaking people

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Trial details

Who runs it
Medical College of Wisconsin
Trial code
NCT06220721
Record updated
20 July 2026
Original description
The long-term goal of our work is to evaluate the effect of intensive postpartum blood pressure control on maternal cardiovascular health, risk of chronic hypertension, and reversal of vascular dysfunction generated by hypertensive disorders of pregnancy, thus attenuating the lifelong trajectory of cardiovascular disease risk.Read full original descriptionShow less

Reducing the Risk of Chronic Hypertension and Improving Vascular Function Following Preeclampsia

The long-term goal of our work is to evaluate the effect of intensive postpartum blood pressure control on maternal cardiovascular health, risk of chronic hypertension, and reversal of vascular dysfunction generated by hypertensive disorders of pregnancy, thus attenuating the lifelong trajectory of cardiovascular disease risk.

Inclusion: Hypertensive disorders of pregnancy (HDP) diagnosis, specifically gestational hypertension, preeclampsia, eclampsia, or HELLP syndrome, according to ACOG guidelines; Postpartum day 0-4; Age ≥ 18 years; Able to communicate in English or in Spanish; Has an established OBGYN at an MCW or NU health system practice that has access to Epic electronic medical records.

Exclusion: Already taking long-acting antihypertensive medication for standard care; Pre-gestational hypertension; Type 1 or type 2 diabetes mellitus; Known allergy or contraindication to nifedipine ER; Maternal conditions that impact study outcomes: sickle cell disease, systemic lupus erythematosus; Admitted to intensive care unit at the time of screening; Diagnosed with HDP during postpartum readmission after discharge from delivery hospitalization; Getting discharged on the day of screening; Inability or unwillingness to provide informed consent.

ClinicalTrials.gov NCT06220721