Collection of Samples From Pregnant Women for the Evaluation of Preeclampsia (Pre-E) Biomarkers
Public ClinicalTrials.gov record NCT02780414. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Study identification
- NCT ID
- NCT02780414
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Lead sponsor
- Progenity, Inc.
- Industry
- Enrollment
- 1,730 participants
Conditions and interventions
Conditions
Interventions
Not listed
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
- Dec 31, 2015
- Primary completion
- Sep 28, 2020
- Completion
- Oct 22, 2020
- Last update posted
- Mar 10, 2022
2016 – 2020
United States locations
- U.S. sites
- 20
- U.S. states
- 17
- U.S. cities
- 20
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Center of Research in Women's Health | Birmingham | Alabama | 35294 | — |
| University of Colorado | Aurora | Colorado | 80045 | — |
| Yale Medical | New Haven | Connecticut | 06520 | — |
| Northwestern | Chicago | Illinois | 60611 | — |
| Indiana University Health Physicians Women's Health | Indianapolis | Indiana | 46202 | — |
| Johns Hopkins Medicine | Baltimore | Maryland | 21287 | — |
| University of Mississippi Medical Center | Jackson | Mississippi | 39216 | — |
| Washington Univ School of Medicine - Dept of OB-GYN | St Louis | Missouri | 63111 | — |
| Winthrop Clinical Trials Center | Mineola | New York | 11501 | — |
| University of North Carolina at Chapel Hill | Chapel Hill | North Carolina | 27599-7516 | — |
| Duke University | Durham | North Carolina | 27705 | — |
| Good Samaritan Hospital | Cincinnati | Ohio | 45220 | — |
| University of Oklahoma | Oklahoma City | Oklahoma | 73104 | — |
| Geisinger Medical Center | Danville | Pennsylvania | 17822 | — |
| Regional Obstetrical Consultants, PC | Chattanooga | Tennessee | 37403 | — |
| Austin Maternal Fetal Medicine | Austin | Texas | 78758 | — |
| University of Texas Medical Branch, Galveston | Galveston | Texas | 77555 | — |
| UT Health Medical School | Houston | Texas | 77030 | — |
| University of Utah Hospital, OB/GYN Dept. | Salt Lake City | Utah | 84132 | — |
| Medical College of Wisconsin - Department of Obstetrics & Gynecology | Milwaukee | Wisconsin | 53226 | — |
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 NCT02780414, 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 Mar 10, 2022 · Synced May 17, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02780414 live on ClinicalTrials.gov.