Sample Collection Study
This is a limited prospective collection of whole blood samples from pregnant women with a diagnosis of preeclampsia with severe features and/or fetal growth restriction in addition to samples from a control group to aid in the development of a Next Generation Sequencing (NGS)-based assay to detect molecular markers associated with preterm preeclampsia.
Study Type
OBSERVATIONAL
Enrollment
242
Christiana Hospital
Newark, Delaware, United States
Tufts Medical Center
Boston, Massachusetts, United States
Saint Peter's University Hospital
New Brunswick, New Jersey, United States
cfRNA markers associated with preeclampsia with severe features and/or fetal growth restrictions
Time frame: 2 years
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Rutgers University
Piscataway, New Jersey, United States
Virtua Materna-Fetal Medicine Specialists
Sewell, New Jersey, United States
New York-Presbyterian/Queens
Flushing, New York, United States
New York-Presbyterian/Columbia University Medical Center
New York, New York, United States
Winthrop University Hospital Clinical Trials Center
New York, New York, United States
Drexel Medicine
Philadelphia, Pennsylvania, United States
The University of Texas Medical Branch
Galveston, Texas, United States