Guideline-directed Management and Therapy (GDMT) for the Prevention of Postpartum Cardiac Dysfunction in Preeclamptic African American Women
Running, not enrolling · Not applicable
Conditions studied: Preeclampsia Postpartum
In brief
This is a single-center, open-label pilot study looking at how Guideline-directed management and therapy (GDMP) in post-partum women with preeclampsia can improve Global Longitudinal Strain (GLS).
Key facts
- Study ID
- NCT05534932
- Run by
- University of Chicago
- People needed
- 20
- Starts
- 2022-10-27
- Expected to finish
- 2026-11-01
- Last updated by the study team
- 2025-11-10
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Adults between 18 and 45 years of age
- African American
- >120/80 BP at the time of their 6-month visit in the PARENT study
- Diagnosed with preeclampsia
- Initially presented to University of Chicago Medical Center (UCMC) for a Singleton Gestation Delivery
- Completed the 6 month visit in the PARENT study
You may not qualify if…
- Those who cannot provide consent
- patients with preexisting cardiomyopathy, ischemic or valvular heart disease, pulmonary disease, diabetes mellitus, chronic kidney disease, multiple gestations,
- Unable to operate the RPM tablet device
Where it is running
- University of Chicago Hospital — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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