Management of Postpartum Preeclampsia (MOPP)
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- STATUS
- Recruiting
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- End date
- Jun 30, 2025
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- participants needed
- 409
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- sponsor
- Rutgers, The State University of New Jersey
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.
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.
Details
| Condition | Postpartum Preeclampsia |
|---|---|
| Treatment | Tight postpartum blood pressure control |
| Clinical Study Identifier | NCT05775744 |
| Sponsor | Rutgers, The State University of New Jersey |
| Last Modified on | 4 April 2023 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
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