Genomic sequencing for healthy-looking fetuses
Part of Genetic & congenital, Women’s health & pregnancy clinical trials.
This study looks at the benefits of doing extra genetic testing (genomic sequencing) on samples from routine prenatal tests like CVS or amniocentesis, specifically for pregnancies where the baby appears normal on ultrasound.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are pregnant with a baby that appears normal on ultrasound (no structural problems).
- You are planning to have a prenatal diagnostic test like CVS or amniocentesis.
- You have already done or are planning to do expanded carrier screening (a blood test for genetic carriers).
- You are willing to have extra genetic testing (genomic sequencing) done on the sample from your diagnostic procedure.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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