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Study identifier: NCT06915792 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

PEACE Trial: Postpartum Evaluation of Antihypertensive Cessation and Efficacy

Condition: Postpartum Hypertension (PPHT)  ·  Sponsor: University of California, Los Angeles

PhasePhase 4
Planned participants110
Who can joinFemale, 18 Years to 64 Years
Healthy volunteersNo

About this study

This randomized controlled trial compares two common medications, labetalol and extended-release nifedipine, to determine which is more effective at managing postpartum high blood pressure. We hypothesize that extended-release nifedipine will better control blood pressure and reduce the need for continued medication beyond six weeks postpartum. The study will enroll 110 postpartum participants, randomly assigning them to one of the two medications, with remote blood pressure monitoring to evaluate treatment effectiveness and inform postpartum hypertension management.

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

Talk to the study team

Tina A Nguyen, MD  ·  310-794-7274  ·  tinaanguyen@mednet.ucla.edu

Sonia S Raghuram, MS  ·  408-896-8704  ·  sraghuram@mednet.ucla.edu

Always discuss trial participation with your own doctor first.

Locations (1)

UCLA Ronald ReaganLos Angeles, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06915792