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Clinical Trial Summary

The purpose of this study is to determine if monitored blood pressure paired with education reduces maternal mortality and morbidity during the post-partum period in a high-risk rural population of women.


Clinical Trial Description

Women with hypertension during pregnancy are at an increased risk of maternal mortality (death during or within 42 days of termination of pregnancy) and hypertension related morbidity. Black women, women with lower education and less access to health care resources also have increased maternal mortality and morbidity. This project will use Bluetooth enabled blood pressure devices to monitor blood pressure in a population of postpartum women at increased risk for maternal mortality and morbidity. We will compare the number of postpartum hypertensive incidences and severities to a population of women who did not have a postpartum blood pressure control intervention. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04570124
Study type Interventional
Source University of Mississippi Medical Center
Contact
Status Completed
Phase N/A
Start date December 14, 2020
Completion date April 30, 2022

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