NCT01429389.

Trial name or title	Specimen collection from pregnant women at increased risk for fetal aneuploidy.
Target condition and reference standard(s)	Target condition: T21. Reference standard: fetal karyotype.
Index and comparator tests	gNIPT.
Starting date	May 2011.
Contact information	Sequenom, Inc.
Aim to study	To develop a prenatal aneuploidy test using ccfDNA from blood samples from pregnant women who have an increased risk indicator/s for fetal chromosomal aneuploidy detection (T21).
Funding source or sponsor of the study	Study funded by Sequenom, Inc.
Information about the authors contacted	No need for further contact.
Notes