Collection of Whole Blood Specimens in Pregnant Women

NCT03590678 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3000

Last updated 2022-05-05

No results posted yet for this study

Summary

To prospectively collect whole blood specimens and clinical data from pregnant women scheduled for an invasive prenatal diagnostic procedure ("invasive procedure"). Specimens will be used for future testing with an investigational NIPT.

Conditions

  • Pregnancy Related

Sponsors & Collaborators

  • Illumina, Inc.

    lead INDUSTRY

Principal Investigators

  • Kathryn Waldrep, MD · Medical City Dallas Hospital

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-13
Primary Completion
2019-08-30
Completion
2019-12-31

Countries

  • United States
  • Australia
  • Malaysia
  • Poland
  • Thailand
  • Ukraine

Study Locations

More Related Trials

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 NCT03590678 on ClinicalTrials.gov