Noninvasive Prenatal Diagnosis: Using Fetal Cells From Maternal Blood
Status unconfirmed
Conditions studied: Chromosome Disorders
In brief
This purpose of this study is to develop noninvasive methods of prenatal diagnosis. Fetal cells can be found in maternal blood. This study is designed to isolate these fetal cells from a sample of the pregnant woman's blood and use those cells to test for fetal chromosome abnormalities.
Key facts
- Study ID
- NCT00064597
- Run by
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
- People needed
- 3500
- Starts
- 1987-12-01
- Expected to finish
- 2003-12-01
- Last updated by the study team
- 2005-06-24
Who can join
Age: 16 and older, up to 45. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Pregnant
- Abnormal serum marker profile (alpha-fetoprotein, hCG, estriol)
- Ultrasound abnormalities of the fetus
- Any high risk indicator for aneuploidy as determined by physician
Where it is running
- University of Illinois at Chicago — Chicago, Illinois, United States
- New England Medical Center Hospital — Boston, Massachusetts, United States
- Wayne State University — Detroit, Michigan, United States
- Jefferson Medical College — Philadelphia, Pennsylvania, United States
- Baylor College of Medicine — Houston, Texas, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.