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Specimen Collection From Pregnant Women at Increased Risk for Fetal Aneuploidy

Recruitingn/aAges 18 Years - anyFemaleSequenom, Inc.
NCT01429389 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The specimen collection is designed for the purpose of the development of a noninvasive prenatal test for T21.

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📋 Eligibility rules (as published)
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
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What it tests

  • Not listed
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Where

14 sites
University of Alabama Birmingham
Birmingham, United States
Cedars-Sinai Medical Center
Los Angeles, United States
Sharp-Rees Stealy Medical Group
San Diego, United States
UCSD
San Diego, United States
Women's Health Care Research
San Diego, United States
Specialty Obstetrics of San Diego
San Diego, United States
Reproductive Genetics Institute
Chicago, United States
University of Iowa Health Care
Iowa City, United States

…and 6 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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