Speedy gene test for fetuses shows promise in pilot study
NCT ID NCT03964441
First seen Feb 03, 2026 · Last updated May 01, 2026 · Updated 14 times
Summary
This study tested whether a fast version of genome sequencing (called exome sequencing) could help doctors find genetic causes for abnormalities seen on prenatal ultrasounds. Researchers enrolled 149 pregnant women whose fetuses had ultrasound findings suggesting a possible genetic condition. The goal was to see how quickly results could be returned and how well the test worked compared to standard methods.
Disclaimer
Read more
Show less
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.
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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for PRENATAL are added.
Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Locations
-
CHU Dijon Bourgogne
Dijon, 21079, France
Conditions
Explore the condition pages connected to this study.