New DNA blood test may spot fetal disorders more accurately in first trimester
NCT ID NCT03375359
First seen Jan 31, 2026 · Last updated Jun 09, 2026 · Updated 16 times
Summary
This study looked at whether a blood test that analyzes fetal DNA (cell-free DNA) can better detect certain genetic conditions—like Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), Patau syndrome (trisomy 13), and 22q11.2 deletion syndrome—during the first trimester of pregnancy. Researchers compared this newer test to the standard combined screening (ultrasound and blood markers) in about 1,000 pregnant women. The goal was to see how often the test gives a false positive or no result, not to treat or prevent any condition.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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University Hospital Tuebingen, Department of Women's Health
Tübingen, 72076, Germany
Conditions
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