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Study identifier: NCT07041281 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Spironolactone to Improve Pregnancy-Associated Hypertension Trajectories

Condition: Preeclampsia · Gestational Hypertension  ·  Sponsor: Massachusetts General Hospital

PhasePhase 2
Planned participants204
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Michael C Honigberg, MD, MPP  ·  617-726-1843  ·  mhonigberg@mgh.harvard.edu

Always discuss trial participation with your own doctor first.

Locations (3)

Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting
Brigham and Women's HospitalBoston, Massachusetts, United StatesRecruiting
University of Pittsburgh Magee-Womens HospitalPittsburgh, Pennsylvania, United StatesNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07041281