Clinical Evaluation of the SEQureDx Trisomy Test in Low Risk Pregnancies

Status Completed

Clinical Trial Summary

Pregnant women with low risk indicators for fetal chromosomal aneuploidy will be enrolled. Study blood will be collected in the first or second trimester at a scheduled prenatal screening visit, processed to plasma, and stored frozen until analysis. Each pregnancy will be followed until delivery and the birth outcome recorded.

Clinical Trial Description

n/a

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01597063
Study type	Observational
Source	Sequenom, Inc.
Contact
Status	Completed
Phase	N/A
Start date	July 2012
Completion date	December 2015

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