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Study identifier: NCT05180773 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Impact of Bromocriptine on Clinical Outcomes for Peripartum Cardiomyopathy

Condition: Peripartum Cardiomyopathy, Postpartum  ·  Sponsor: Dennis M. McNamara, MD, MS

PhasePhase 4
Planned participants250
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The study will enroll 200 women newly diagnosed with peripartum cardiomyopathy within 5 months postpartum in a randomized placebo controlled trial of bromocriptine therapy to evaluate its impact on myocardial recovery and clinical outcomes. Given that bromocriptine prevents breastfeeding, an additional 50 women with peripartum cardiomyopathy excluded from the trial due to a desire to continue breastfeeding but meeting all other entry criteria will be followed in an observational cohort.

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

Talk to the study team

Dennis McNamara, MD  ·  412-802-3131  ·  mcnamaradm@upmc.edu

Always discuss trial participation with your own doctor first.

Locations (64)

University of Alabama BirminghamBirmingham, Alabama, United StatesRecruiting
University of Arizona Sarver Heart CenterTucson, Arizona, United StatesRecruiting
University of California San DiegoLa Jolla, California, United StatesRecruiting
Keck School of Medicine of USCLos Angeles, California, United StatesRecruiting
Cedars-Sinai Medical CenterLos Angeles, California, United StatesRecruiting
University of California Irvine HealthOrange, California, United StatesRecruiting
Stanford UniversityStanford, California, United StatesRecruiting
University of Colorado Anschutz Medical CampusAurora, Colorado, United StatesRecruiting
Hartford HospitalHartford, Connecticut, United StatesRecruiting
Yale UniversityNew Haven, Connecticut, United StatesRecruiting
University of FloridaGainesville, Florida, United StatesRecruiting
Mayo Clinic, FloridaJacksonville, Florida, United StatesRecruiting

+ 52 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05180773