drugset / Trial / NCT07041281

Spironolactone to Improve Pregnancy-Associated Hypertension Trajectories

NCT07041281

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The hypertensive disorders of pregnancy (preeclampsia and gestational hypertension) are associated with increased long-term maternal risk of developing cardiovascular disease. Recent evidence suggests that activation of the mineralocorticoid receptor promotes ongoing susceptibility to hypertension in women following hypertensive disorders of pregnancy. In addition, women with overweight/obesity are at increased risk for progression to chronic hypertension after experiencing hypertensive disorders of pregnancy. Among women with hypertensive disorders of pregnancy and pre-pregnancy overweight/obesity, the investigators will conduct a randomized trial to test the effect of pharmacologically blocking the mineralocorticoid receptor for three months after delivery on blood pressure and cardiac remodeling at nine months postpartum.

Timeline

Start
2025-10-16
Primary completion
2027-12-02
Completion
2029-03-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Spironolactone Small molecule 25 mg Oral

Indications