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RECRUITING
NCT01429389

Specimen Collection from Pregnant Women At Increased Risk for Fetal Aneuploidy

Sponsor: Sequenom, Inc.

View on ClinicalTrials.gov

Summary

The specimen collection is designed for the purpose of the development of a noninvasive prenatal test for T21.

Official title: Collection of Whole Blood Specimens from Pregnant Women At Increased Risk of Fetal Chromosomal Abnormality for Use in Development of a Noninvasive Prenatal Test in the Detection of the Relative Quantity of Chromosomal Material in Circulating Cell-Free DNA Extracted from Maternal Plasma

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

2000

Start Date

2011-05

Completion Date

2026-03

Last Updated

2024-10-16

Healthy Volunteers

No

Locations (14)

University of Alabama Birmingham

Birmingham, Alabama, United States

Cedars-Sinai Medical Center

Los Angeles, California, United States

Sharp-Rees Stealy Medical Group

San Diego, California, United States

UCSD

San Diego, California, United States

Women's Health Care Research

San Diego, California, United States

Specialty Obstetrics of San Diego

San Diego, California, United States

Reproductive Genetics Institute

Chicago, Illinois, United States

University of Iowa Health Care

Iowa City, Iowa, United States

Henry Ford Hospital

Detroit, Michigan, United States

Spectrum Health

Grand Rapids, Michigan, United States

The Cooper Health System

Camden, New Jersey, United States

Medical University of South Carolina

Charleston, South Carolina, United States

IWK Health Centre

Halifax, Nova Scotia, Canada

North York General Hospital

Toronto, Ontario, Canada