Management of Postpartum Preeclampsia
Completed · Not applicable
Conditions studied: Postpartum Preeclampsia
In brief
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.
Key facts
- Study ID
- NCT05775744
- Run by
- Rutgers, The State University of New Jersey
- People needed
- 392
- Starts
- 2023-03-28
- Expected to finish
- 2024-03-26
- Last updated by the study team
- 2024-04-02
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Chronic hypertension, gestational hypertension, or preeclampsia.
- Delivery of a neonate after 20 weeks during their current hospitalization
- Able to consent
- 18 years old or above
- English or Spanish speaking
- Planning to follow up with a physician associated with Robert Wood Johnson University Hospital or Cooperman Barnabas Medical Center
- Ability to follow directions
You may not qualify if…
- Any medical condition that the providers feel is a contraindication to the MOPP algorithm.
- Planning to follow up with an outside institution.
- Unwillingness to take blood pressure at home.
Where it is running
- Cooperman Barnabas Medical Center — Livingston, New Jersey, United States
- Robert Wood Johnson Medical School — New Brunswick, New Jersey, United States
Full record on ClinicalTrials.gov
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