Last updated on February 2018

Whole Blood Specimen Collection From Pregnant Subjects


Brief description of study

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

Detailed Study 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.

Clinical Study Identifier: NCT02430584

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C. David Adair, MD

Regional Obstetrical Consultants
Chattanooga, TN United States
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