Whole Blood Specimen Collection From Pregnant Subjects

Status Active, not recruiting

Clinical Trial Summary

To obtain whole blood specimens from pregnant subjects to be used for research and development and clinical validation studies of prenatal assays.

Clinical Trial Description

This sample collection protocol allows for the identification, recruitment, and participation in women who are pregnant and are known to:

1. be at an increased risk for fetal genetic abnormalities

2. be at increased risk for congenital fetal infection by virtue of being positive by initial screening tests, or are known to have an active infection during this pregnancy.

3. possess irregular blood group antigens (the subject or the father of the baby) and are therefore at increased risk for fetal sensitization during this pregnancy. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02430584
Study type	Observational
Source	Progenity, Inc.
Contact
Status	Active, not recruiting
Phase
Start date	March 2015
Completion date	May 2021

View Details

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