Whole blood sample procurement study from pregnant women with signs and symptoms of Preeclampsia.
This multicenter non-interventional observational sample acquisition study is designed to acquire whole-blood samples from pregnant women who present with signs and symptoms of Pre-E and are in the care at an OB-GYN and/or Maternal Fetal Medicine (MFM) site, defined as outpatient centers, clinic sites, and medical offices. Study population includes subjects who are pregnant, of any race or ethnicity, 18 to 45 years of age, 28 0/7 to 36 6/7 weeks' gestational age with a singleton fetus and have provided written informed consent to provide whole blood specimens at one or more study visits.
Study Type
OBSERVATIONAL
Enrollment
344
This is an observational, non-interventional study.
West Coast Medical Research, Inc.
San Diego, California, United States
Diagnosis of preeclampsia is determined by standard of care.
Observational, non-interventional sample procurement study in which participants are treated per standard of care
Time frame: 3 months
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