Quick gene test for unborn babies could speed up diagnosis
NCT ID NCT05834621
First seen Nov 01, 2025 · Last updated May 23, 2026 · Updated 28 times
Summary
This study was designed to see if a rapid whole genome sequencing test on amniotic fluid can diagnose genetic conditions in fetuses faster than current methods. Researchers planned to compare results from amniotic fluid and blood samples from up to 90 families. However, the study was withdrawn before enrolling any participants.
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 MULTIPLE ANOMALIES OF FETUS are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
Explore the condition pages connected to this study.