TerminatedPhase 3NCT03944512
Pravastatin to Prevent Preeclampsia
Studying Preeclampsia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- The George Washington University Biostatistics Center
- Principal Investigator
- Maged Costantine, MDOhio State University
- Intervention
- Pravastatin(drug)
- Enrollment
- 102 target
- Eligibility
- 16 years · FEMALE
- Timeline
- 2019 – 2024
Study locations (12)
- University of Alabama - Birmingham, Birmingham, Alabama, United States
- Northwestern University, Chicago, Illinois, United States
- Columbia University, New York, New York, United States
- University of North Carolina - Chapel Hill, Chapel Hill, North Carolina, United States
- Case Western Reserve-Metro Health, Cleveland, Ohio, United States
- Ohio State University Hospital, Columbus, Ohio, United States
- Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
- Magee Women's Hospital of UPMC, Pittsburgh, Pennsylvania, United States
- Brown University, Providence, Rhode Island, United States
- University of Texas Medical Branch, Galveston, Texas, United States
- University of Texas - Houston, Houston, Texas, United States
- University of Utah Medical Center, Salt Lake City, Utah, United States
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) · National Heart, Lung, and Blood Institute (NHLBI)
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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