Noninvasive Screening for Fetal Aneuploidy: A New Maternal Plasma Marker

Status Completed

Clinical Trial Summary

The purpose of this study is to collect samples for the purpose of developing a prenatal aneuploid test using circulating cell free fetal (ccff) nucleic acid from blood samples from pregnant women who have a high-risk pregnancy undergoing invasive prenatal diagnosis by chorionic villus sampling (CVS) and/or genetic amniocentesis. The results of the ccff aneuploid test will be compared to the chromosomal analysis obtained via CVS or amniocentesis.

Clinical Trial Description

n/a

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00971334
Study type	Observational
Source	Sequenom, Inc.
Contact
Status	Completed
Phase	N/A
Start date	August 2009
Completion date	December 2011

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