Development of a Fetal Sex Assay From Maternal Whole Blood

NCT00970047 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2011-02-02

No results posted yet for this study

Summary

Whole blood from pregnant women will be collected to develop a noninvasive fetal sex test.

Conditions

  • Fetal Sex Determination

Sponsors & Collaborators

  • Sequenom, Inc.

    lead INDUSTRY

Principal Investigators

  • Allan Bombard, MD, MBA · Sequenom, Inc.

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2010-07-31
Completion
2010-07-31

Countries

  • United States

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 NCT00970047 on ClinicalTrials.gov