Fetal Jeopardy and Congenital Anomalies Study

The Combination of Biochemical Markers and Two & Three-Dimensional Ultrasound Using Geometric Morphometrics in the Identification of Fetal Jeopardy and Congenital Anomalies

Protocol ID

07-077

Protocol Description

The purpose of the study is to evaluate whether a combination of blood tests, early ultrasound, and 3D ultrasound of the face at 20 weeks gestation can identify fetuses with congenital anomalies, and predict maternal or fetal complications. The other purpose of the study is to determine if screening for chromosomal disorders at the 20 weeks ultrasound is no longer necessary, if all tests before that are normal.  With the exception of a 3D image of the face, both the blood tests and the 2D ultrasounds are a standard part of obstetrical care.

Eligibility Criteria

Pregnant women scheduled to have a routine second trimester ultrasound performed

Primary Investigator(s)

  • Burton Rochelson, MD

Contact Information

Stephanie A. Augustine, RNC
(516) 562-2895
saugustine@nshs.edu

Last Update

January 17, 2012
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