Specimen Collection from Pregnant Women At Increased Risk for Fetal Aneuploidy

NCT01429389 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2024-10-16

No results posted yet for this study

Summary

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

Conditions

  • Down Syndrome
  • Fetal Aneuploidy

Sponsors & Collaborators

  • Sequenom, Inc.

    lead INDUSTRY

Principal Investigators

  • Daniel Grosu, MD · Sequenom, Inc.

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2025-12-31
Completion
2026-03-31

Countries

  • United States
  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01429389 on ClinicalTrials.gov