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Clinical Trial Summary

The objective of this project is the non-invasive prenatal detection of placenta-limited aneuploidies, in patients whose fetuses have a intrauterine growth restriction below 3rd percentile, in parallel with an amniocentesis. This study will allow the chromosomal study of the placenta in pregnant women whose genetic prenatal diagnosis, made by amniocentesis, does not allow exploring the placental causes of fetal RCIU.


Clinical Trial Description

Placental chromosomal aneuploidies will be detected by high-throughput whole genome sequencing of non-cellular DNA present in maternal plasma during pregnancy. The study of the cfDNA will be carried out from a blood sample with the automated solution VERISEQ NIPT (Illumina) using the software illumina VeriSeq v2, allowing the detection of all chromosomal abnormalities. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05023161
Study type Observational
Source University Hospital, Bordeaux
Contact Caroline THAMBO
Phone 05 56 79 59 52
Email caroline.rooryck-thambo@chu-bordeaux.fr
Status Recruiting
Phase
Start date October 5, 2021
Completion date October 5, 2024

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