Noninvasive In Vitro Diagnostic Test For Fetal Chromosomal Abnormality: Assay Development and Optimization in Affected Pregnancies with Abnormal Microarray Findings
Sponsor: |
Sequenom, Inc |
Enrolling: |
Female Patients Only |
IRB Number: |
AAAN9002 |
U.S. Govt. ID: |
NCT01052688 |
Contact: |
Amita Russel: 855-772-7729 / abr2143@columbia.edu |
The purpose of this study is to collect blood samples from women who are pregnant with a fetus that has been confirmed by prenatal microarray testing to have a chromosomal abnormality, such as a microdeletion (missing chromosomes) or microduplication (extra chromosomes). The sponsor of this study, Sequenom Laboratories, will use these samples to develop and optimize a noninvasive blood test that could identify such abnormalities in other women without the need for an invasive procedure.
This study is closed
Investigator
Ronald Wapner, MD
Are you carrying a fetus with a diagnosed chromosomal abnormality? |
Yes |
No |
Are you willing to have your blood taken throughout the study? |
Yes |
No |
Are you between 8-36 weeks pregnant? |
Yes |
No |