Can rapid gene tests spot fetal problems sooner?
NCT ID NCT03964441
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study explores whether a fast type of genome sequencing can help diagnose genetic conditions in fetuses with ultrasound abnormalities. Researchers will take samples from 149 pregnant women and their partners to analyze fetal DNA. The goal is to see if this approach can provide quicker and more detailed results than current methods.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this could show that rapid genome sequencing is feasible in prenatal care, potentially improving diagnosis of genetic conditions during pregnancy.
- What could go wrong
- This is a small feasibility study, not a treatment trial. It may not lead to immediate clinical changes, and results may not apply to all pregnancies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for GENOME-WIDE HIGH THROUGHPUT SEQUENCING are added.
By submitting, you agree to our Terms of use
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
CHU Dijon Bourgogne
Dijon, 21079, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.