UnknownNCT03767803
Collection of Whole Blood Samples for the Evaluation of Preeclampsia (Pre-E) Biomarkers From Pregnant Women
Studying Cerebral visual impairment
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
- Progenity, Inc.
- Principal Investigator
- Peter Stiegler, PhDProgenity, Inc.
- Intervention
- Non-interventional study(other)
- Enrollment
- 344 enrolled
- Eligibility
- 18-45 years · FEMALE
- Timeline
- 2018 – 2020
Study locations (24)
- West Coast Medical Research, Inc., San Diego, California, United States
- Christiana Care, Newark, Delaware, United States
- Women's Health Partners, LLC, Boca Raton, Florida, United States
- Discovery Clinical Research, Plantation, Florida, United States
- Leavitt Clinical Research, Idaho Falls, Idaho, United States
- Norton Healthcare, Louisville, Kentucky, United States
- Obstetrics and Gynecology Associates AMB, Silver Spring, Maryland, United States
- Valley OB-GYN Clinic, PC, Saginaw, Michigan, United States
- Rutgers-RWJMS, New Brunswick, New Jersey, United States
- St. Peter's University Hospital, New Brunswick, New Jersey, United States
- Virtua Voorhees Hospital, Voorhees Township, New Jersey, United States
- New Life Medical Esthetics and Wellness, PLLC, Brooklyn, New York, United States
- Columbia University, New York, New York, United States
- Total Woman Care, Elkin, North Carolina, United States
- David B. Schwartz, MD, LLC, Cincinnati, Ohio, United States
- +9 more locations on ClinicalTrials.gov
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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