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Management of Postpartum Preeclampsia — MOPP  

Postpartum Preeclampsia Clinical Trial

Official title:
Management of Postpartum Preeclampsia

Clinical Trial Summary

The aim of this study is to assess the effect of a lower treatment threshold for antihypertensive medication and tighter blood pressure control, using remote blood pressure monitoring, on reducing Emergency Room visits for our postpartum patients with hypertensive disease.

Clinical Trial Description

The aim of this study is to assess the effect of lower treatment threshold for initiating antihypertensive medication and tighter blood pressure control, using remote blood pressure monitoring, on reducing Emergency Room visits for our postpartum patients with hypertensive disease. The investigators will study and compare two cohorts of patients. The first is a retrospective cohort, including patients delivered at Robert Wood Johnson University Hospital and Cooperman Barnabas Medical Center. The second is a prospective cohort that will enroll patients immediately postpartum who are eligible for our treatment protocol. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05775744
Study type Interventional
Source Rutgers, The State University of New Jersey
Contact
Status Completed
Phase N/A
Start date March 28, 2023
Completion date March 26, 2024
View Details
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