Noninvasive In Vitro Diagnostic Test For Fetal Chromosomal Abnormality: Assay Development and Optimization in Affected Pregnancies with Abnormal Microarray Findings
A study for pregnant women to test fetal chromosomal abnormality
Sponsor: Sequenom, Inc
Enrolling: Female Patients Only
IRB Number: AAAN9002
U.S. Govt. ID: NCT01052688
Contact: Amita Russel: 855-772-7729 / abr2143@columbia.edu
Additional Study Information: 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
Do You Qualify?
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
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You may be eligible for this study

Place Holder




For more information, please contact:
Amita Russel
abr2143@columbia.edu
855-772-7729