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NCT05775744 · ClinicalTrials.gov registry record · NA
Management of Postpartum Preeclampsia
A NA study of Postpartum Preeclampsia, sponsored by Rutgers, The State University of New Jersey.
- Completed
- Registry status
- NA
- Development phase
- 392
- Enrollment target
- 2
- Study locations
NCT05775744 is a NA study of Postpartum Preeclampsia that has completed, run by Rutgers, The State University of New Jersey. The registered enrollment target is 392 participants, below the 498-participant average among 5 other Postpartum Preeclampsia trials with a reported enrollment target (21% lower). The trial reports 2 study locations across 1 state.
The verdict
NCT05775744, a NA study of Postpartum Preeclampsia, has completed, sponsored by Rutgers, The State University of New Jersey.
- COMPLETED
- Registry status
- NA
- Development phase
- 392 participants
- Enrollment target
- 2
- Study locations
Study 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.
Conditions Studied
Interventions
- OTHER Tight postpartum blood pressure control
Study Locations (2)
New Jersey
- Cooperman Barnabas Medical Center - Livingston
- Robert Wood Johnson Medical School - New Brunswick
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 392 participants |
| Start Date | 2023-03-28 |
| Est. Completion | 2024-03-26 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05775744
The ClinicalTrials.gov registry entry for NCT05775744 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 392 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 498-participant average among 5 other Postpartum Preeclampsia trials with a reported enrollment target (21% lower). The listed sponsor is Rutgers, The State University of New Jersey, which has 413 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Postpartum Preeclampsia appearing as the primary indexed condition, and to 1 intervention - of which Tight postpartum blood pressure control is the first listed.
NCT05775744 reports 2 study locations spanning 1 distinct geographic area - top geographies include New Jersey.
Frequently Asked Questions
What is clinical trial NCT05775744 about?
NCT05775744 is a clinical study titled "Management of Postpartum Preeclampsia". 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.
What is the current status of trial NCT05775744?
This trial is currently completed. It is a NA study. The enrollment target is 392 participants. The study started on 2023-03-28. Estimated completion is 2024-03-26.
What conditions does trial NCT05775744 study?
This clinical trial studies the following conditions: Postpartum Preeclampsia.
What interventions are being tested in trial NCT05775744?
The interventions under investigation include: Tight postpartum blood pressure control (OTHER).
Who is sponsoring clinical trial NCT05775744?
This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05775744 being conducted?
This trial has 2 study locations across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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