CompletedNot applicableNCT05775744
Management of Postpartum Preeclampsia
Studying Preeclampsia
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Rutgers, The State University of New Jersey
- Principal Investigator
- Deepika Sagaram, MDRutgers, Robert Wood Johnson
- Intervention
- Tight postpartum blood pressure control(other)
- Enrollment
- 392 enrolled
- Eligibility
- 18 years · FEMALE
- Timeline
- 2023 – 2024
Study locations (2)
- Cooperman Barnabas Medical Center, Livingston, New Jersey, United States
- Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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