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Not listed No phase listed Observational

Collection of Whole Blood Samples for the Evaluation of Preeclampsia (Pre-E) Biomarkers From Pregnant Women

ClinicalTrials.gov ID: NCT03767803

Public ClinicalTrials.gov record NCT03767803. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 8:42 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Collection of Whole Blood Samples for the Evaluation of Preeclampsia (Pre-E) Biomarkers

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Whole blood sample procurement study from pregnant women with signs and symptoms of Preeclampsia.

Study identification

NCT ID
NCT03767803
Recruitment status
Not listed
Study type
Observational
Phase
Not listed
Lead sponsor
Progenity, Inc.
Industry
Enrollment
344 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 45 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 1, 2018 (Actual)
Primary completion
Dec 31, 2020 (Estimated)
Completion
Dec 31, 2020 (Estimated)
Last update posted
Jan 23, 2020

2018 – 2020

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
West Coast Medical Research, Inc. San Diego California 92123 —
Christiana Care Newark Delaware 19718 —
Women's Health Partners, LLC Boca Raton Florida 33433 —
Discovery Clinical Research Plantation Florida 33324 —
Leavitt Clinical Research Idaho Falls Idaho 83404 —
Norton Healthcare Louisville Kentucky 40202 —
Obstetrics and Gynecology Associates AMB Silver Spring Maryland 20910 —
Valley OB-GYN Clinic, PC Saginaw Michigan 48602 —
Rutgers-RWJMS New Brunswick New Jersey 08901 —
St. Peter's University Hospital New Brunswick New Jersey 08901 —
Virtua Voorhees Hospital Voorhees Township New Jersey 08043 —
New Life Medical Esthetics and Wellness, PLLC Brooklyn New York 11220 —
Columbia University New York New York 10032 —
Total Woman Care Elkin North Carolina 28621 —
David B. Schwartz, MD, LLC Cincinnati Ohio 45219 —
Obstetrics & Gynecology Associates, Inc. Fairfield Ohio 45014 —
Hilltop Obstetrics & Gynecology Franklin Ohio 45005 —
Dr. Ahuja and Associates OB-GYN Mentor Ohio 44060 —
Drexel University Philadelphia Pennsylvania 19102 —
The Jackson Clinic, PA Jackson Tennessee 38305 —
Aa Ob-Gyn, Pllc Austin Texas 78758 —
OB-GYN North Austin Texas 78758 —
Corpus Christi Women's Clinic Corpus Christi Texas 78412 —
Advanced Clinical Research Salt Lake City Utah 84107 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03767803, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 23, 2020 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03767803 live on ClinicalTrials.gov.

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