๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2024-10-11

Specimen Collection from Pregnant Women At Increased Risk for Fetal Aneuploidy (NCT01429389)

Collection of Whole Blood Specimens from Pregnant Women At Increased Risk of Fetal Chromosomal Abnormality for Use in Development of a Noninvasive Prenatal Test in the Detection of the Relative Quantity of Chromosomal Material in Circulating Cell-Free DNA Extracted from Maternal Plasma

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: Sequenom, Inc.

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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

Who can join: Review the eligibility criteria below.

Location: University of Alabama Birmingham โ€” Birmingham, Alabama

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (14 Sites)

  • University of Alabama Birmingham โ€” Birmingham, Alabama
  • Cedars-Sinai Medical Center โ€” Los Angeles, California
  • Sharp-Rees Stealy Medical Group โ€” San Diego, California
  • UCSD โ€” San Diego, California
  • Women's Health Care Research โ€” San Diego, California
  • Specialty Obstetrics of San Diego โ€” San Diego, California
  • Reproductive Genetics Institute โ€” Chicago, Illinois
  • University of Iowa Health Care โ€” Iowa City, Iowa
  • Henry Ford Hospital โ€” Detroit, Michigan
  • Spectrum Health โ€” Grand Rapids, Michigan
  • The Cooper Health System โ€” Camden, New Jersey
  • Medical University of South Carolina โ€” Charleston, South Carolina
  • IWK Health Centre โ€” Halifax, Nova Scotia
  • North York General Hospital โ€” Toronto, Ontario

๐Ÿ“ž Contact the Study Coordinator

Phone: (205) 934-5509

Email: rachel.copper@obgyn.uab.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

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๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—