New DNA test aims to solve mysteries of severe fetal malformations
NCT ID NCT02512354
Summary
This study tested whether a new, advanced DNA test could find the cause when a fetus has multiple serious malformations and standard exams fail. Researchers performed this test on 100 fetuses with at least two malformations, along with blood samples from both parents, to see if it provided answers where other methods could not. The goal was to see if this technology could improve diagnosis for families facing these difficult and unexplained pregnancies.
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 FETUSES WITH AT LEAST 2 MALFORMATIONS, AND NO DIAGNOSIS AFTER FETOPATHOLOGICAL AND RADIOLOGICAL EXAMINATIONS are added.
By submitting, you agree to our Terms of use
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
-
CH de Mulhouse (Hôpital Emile Muller)
Mulhouse, 68070, France
-
CHRU de Reims (Hôpital Maison Blanche)
Reims, 51092, France
-
CHRU de Tours
Tours, 37000, France
-
CHU Montpellier
Montpellier, 34000, France
-
CHU de Clermont-Ferrand
Clermont-Ferrand, 63000, France
-
CHU de DIJON
Dijon, 21079, France
-
CHU de NANCY
Vandœuvre-lès-Nancy, 54511, France
-
CHU de Rennes
Rennes, 35203, France
-
CHU de Rouen
Rouen, 76000, France
-
CHU de STRASBOURG (Hôpital Hautepierre)
Strasbourg, 67098, France
Conditions
Explore the condition pages connected to this study.