Clinical Evaluation of the SEQureDx T21 Test In High Risk Pregnancies

NCT01555346 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3062

Last updated 2016-04-20

No results posted yet for this study

Summary

Whole blood samples will be collected from high-risk pregnant women to validate the clinical performance of the SEQureDx Trisomy 21 Test.

Conditions

  • Down Syndrome
  • Fetal Aneuploidy

Sponsors & Collaborators

  • Sequenom, Inc.

    lead INDUSTRY

Principal Investigators

  • Juan-Sebastian Saldivar, MD · Sequenom Laboratories

Eligibility

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

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2014-10-31
Completion
2015-12-31

Countries

  • United States
  • Canada

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 NCT01555346 on ClinicalTrials.gov