RecruitingPreeclampsia (PE)
Non-Invasive Preeclampsia Screening and Biobank
Eligible age
18+ yrs
Accepts
Women
Locations
12 states
Healthy volunteers
Yes
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
Women pregnant between 11-14 weeks gestation will be enrolled with blood samples collected to evaluate for preeclampsia.
Sponsor: Sequenom, Inc.
You may qualify if…
- ✓ Subject is female and 18 years of age and older;
- ✓ Subject provides a signed and dated informed consent;
- ✓ Subject is pregnant with a singleton pregnancy at ≥11.0 - ≤14.0 weeks' gestation;
- ✓ Subject agrees to provide the Sponsor access to any prenatal and postnatal screening or diagnostic test results and supporting data;
- ✓ Subject agrees to have UtAPI calculated during their SOC first trimester ultrasound and MAP collected at the first trimester SOC visit;
- ✓ Subject agrees to provide up to 25mL of whole blood at each trimester visit;
- ✓ Subject agrees to provide relevant medical and pregnancy/postnatal information including outcome.
You may not qualify if…
- ✕ Subject is unlikely to return for second and third trimester testing;
- ✕ Subject is unlikely to have pregnancy outcome data available;
- ✕ Previous sample donation under this protocol with the same pregnancy;
- ✕ Subject is participating in a blinded aspirin study or taking unknown doses of aspirin.
Where it's recruiting
Arizona
Glendale
Delaware
Newark
Florida
Miami
Louisiana
Metairie
Massachusetts
Boston
New Jersey
Camden · Livingston · New Brunswick · Pennington
New York
New York
North Carolina
Winston-Salem
Pennsylvania
Danville · Philadelphia
Tennessee
Chattanooga
Texas
Austin · Galveston · Houston
Virginia
Norfolk
Source: ClinicalTrials.gov · NCT06643741 · last updated 2026-06-11