Non-Invasive Determination of Fetal Chromosome Abnormalities

Conditions:		Down Syndrome (Trisomy 21) - Edward's Syndrome (Trisomy 18) - Patau Syndrome (Trisomy 13) - Klinefelter Syndrome (47, XXY) - and Other Chromosome - Abnormalities.
Purpose:		The overall significance of this study is to develop a laboratory developed test (LDT) to use a new marker in the maternal blood to better identify pregnancies that have a child with a chromosome abnormality such as Down syndrome (trisomy 21), Edward's syndrome (trisomy 18), Patau syndrome (trisomy 13), Klinefelter syndrome, (47, XXY), and other chromosome abnormalities. Accomplishing that task would reduce the need for invasive amniocentesis and CVS procedures.
Study Summary:
Criteria:		Inclusion Criteria: - This study is only applicable to women who are between 8 and 30 weeks' gestation and who have been determined increased risk for fetal aneuploidy. In the interest of expediting and simplifying this study, the investigators want only women who have already decided to undergo second-trimester amniocentesis or CVS. Exclusion Criteria: - The only exclusion criteria are those mentioned.
NCT ID:		NCT00891852
Primary Contact:		Principal Investigator Stephen A Brown, MD Lenetix, Inc.
Backup Contact:		N/A
Location Contact:		Burlington, Vermont 05405 United States Stephen A Brown, MD Phone: 802-656-4775 Email: stephen.brown@uvm.edu Site Status: Recruiting

Data Source:		ClinicalTrials.gov
Date Processed:		May 25, 2013
Modifications to this listing:		Only selected fields are shown, please use the link below to view all information about this clinical trial.
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