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NCT01429389
Specimen Collection From Pregnant Women at Increased Risk for Fetal Aneuploidy
Conditions: Down Syndrome, Fetal Aneuploidy
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 2000
Sponsor: Sequenom, Inc.
Location: University of Alabama Birmingham Birmingham Alabama
Summary
The specimen collection is designed for the purpose of the development of a noninvasive prenatal test for T21.
Eligibility Criteria
Inclusion Criteria:
* pregnant between 10 and 22 weeks gestation
* 18 years of age or older
* provides signed and dated informed consent
* subject is at increased risk for fetal aneuploidy
* subject is willing to undergo a CVS and/or amniocentesis procedure for the purpose of genetic analysis
* subject agrees to provide the genetic results of the invasive procedure
Exclusion Criteria:
* Fetal demise at time of specimen sampling
* Previous sample donation under this protocol
Source: ClinicalTrials.gov (NCT01429389). StuddyBuddy aggregates publicly available trial information.