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RecruitingPreeclampsia (PE)

Non-Invasive Preeclampsia Screening and Biobank

Eligible age

18+ yrs

Accepts

Women

Locations

12 states

Healthy volunteers

Yes

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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

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