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Noninvasive Screening for Affected Pregnancies: Assay Development & Optimization in Affected Pregnancies — CHARMM-AP  

Down Syndrome Clinical Trial

Official title:
Noninvasive Screening for Fetal Chromosomal Aneuploidy and Abnormality: Assay Development & Optimization in Affected Pregnancies

Clinical Trial Summary

To collect samples for the purpose of developing and optimizing an in vitro noninvasive prenatal diagnostic (NIPD) test. The NIPD test employs circulating cell free (ccff) DNA extracted from whole blood samples collected from women who are pregnant with a fetus previously determined to have a chromosomal abnormality. The NIPD result will be compared to the standard test results obtained from other test methods such as karyotype, FISH, QF-PCR, and/or any commercially available NIPD test.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01052688
Study type Observational
Source Sequenom, Inc.
Contact
Status Completed
Phase
Start date November 2009
Completion date August 31, 2021
View Details
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