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Development of a Non-invasive Prenatal Test
Development of a Non-invasive Prenatal Test

NCT01451684

CompletedN/A

Sponsor: Cindy Cisneros

Conditions: Pregnancy

Countries: United States

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.

Eligibility overview

Sex: FEMALE

Age: 18 Years to —

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

* 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

Exclusion Criteria:

* Subject is pregnant with more than two fetuses
* Subject is unwilling to undergo a blood draw
Locations (1)
  • San Jose, California, United States