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NCT06643741 · ClinicalTrials.gov registry record

Non-Invasive Preeclampsia Screening and Biobank

A clinical trial of Preeclampsia (PE), sponsored by Sequenom.

Recruiting
Registry status
6,550
Enrollment target
20
Study locations

NCT06643741 is a study of Preeclampsia (PE) that is actively recruiting participants, run by Sequenom. The registered enrollment target is 6,550 participants. The trial reports 20 study locations across 11 states.

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The verdict

NCT06643741, a study of Preeclampsia (PE), is actively recruiting participants, sponsored by Sequenom.

RECRUITING
Registry status
6,550 participants
Enrollment target
20
Study locations

Study Summary

Women pregnant between 11-14 weeks gestation will be enrolled with blood samples collected to evaluate for preeclampsia.

Conditions Studied

Study Locations (20)

New Jersey

  • Cooper University Health Care - Camden
  • New Jersey Perinatal Associates - Livingston
  • Rutgers Robert Wood Johnson Medical School - New Brunswick
  • Capital Health - Pennington

Texas

  • St. David's Women's Center of Texas - Austin
  • University of Texas Medical Branch - Galveston
  • UT Health - Houston
  • HCA Healthcare, Texas Maternal Fetal Medicine - Houston

Pennsylvania

  • Geisinger Medical Center - Danville
  • University of Pennsylvania Perelman School of Medicine - Philadelphia
  • Lewis Katz School of Medicine at Temple University - Philadelphia

New York

  • Columbia University Medical Center - New York
  • Lenox Hill Hospital - New York

Arizona

  • Valley Perinatal - Glendale

Delaware

  • Delaware Center for Maternal and Fetal Medicine - Newark

Florida

  • D&H National Research Centers - Miami

Louisiana

  • Southern Clinical Research Associates - Metairie

Trial Details

FieldValue
Enrollment Target 6,550 participants
Start Date 2025-02-02
Est. Completion 2026-07-01

Sponsor

Sequenom

26 total trials

What the Registry Record Tells You About NCT06643741

The ClinicalTrials.gov registry entry for NCT06643741 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 6,550 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sequenom, which has 26 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Preeclampsia (PE) appearing as the primary indexed condition, and to 0 interventions.

NCT06643741 reports 20 study locations spanning 11 distinct geographic areas - top geographies include New Jersey, Texas, Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT06643741 about?

NCT06643741 is a clinical study titled "Non-Invasive Preeclampsia Screening and Biobank". Women pregnant between 11-14 weeks gestation will be enrolled with blood samples collected to evaluate for preeclampsia.

What is the current status of trial NCT06643741?

This trial is currently recruiting. The enrollment target is 6,550 participants. The study started on 2025-02-02. Estimated completion is 2026-07-01.

What conditions does trial NCT06643741 study?

This clinical trial studies the following conditions: Preeclampsia (PE).

Who is sponsoring clinical trial NCT06643741?

This trial is sponsored by Sequenom, which has 26 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06643741 being conducted?

This trial has 20 study locations across Arizona, Delaware, Florida, Louisiana, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.