Development of a Non-invasive Prenatal Test

Completed

Conditions studied: Pregnancy

In brief

This is an observational study to aid in the development of a non-invasive prenatal test that may be used to aid in detection of fetal aneuploidy. Pregnant women will be recruited and asked to provide a blood sample to be used for general test development purposes.

Key facts

Study ID

NCT01451684

Run by

Cindy Cisneros

People needed

15000

Starts

2011-06-01

Expected to finish

2019-12-01

Last updated by the study team

2020-04-30

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Subject has singleton or twin pregnancy confirmed via evaluation by a healthcare provider
• Subject is able to provide informed consent
• Subject is ≥ 18 years of age
• Subject is at least 10 weeks gestation for general enrollment
• Subject has no known risk factors for chromosomal abnormalities of the fetus
• Subject has no suspected or confirmed fetal abnormalities

You may not qualify if…

• Subject is pregnant with more than two fetuses
• Subject is unwilling to undergo a blood draw

Where it is running

• Ariosa Diagnostics — San Jose, California, United States

Full record on ClinicalTrials.gov

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