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Clinical Trial Summary

Several molecular studies showed chromosomal alterations in patients with endometrial cancer, with gains in 1q, 19p, 19q, 8q, 10q and 10p and loss of 4q, 16q and 18q. Several genes of interest have been identified (P53, PTEN, PIK3CA, ß-catenin, K-ras ...).

A study has already been carried out at the Reims University Hospital with inclusion of patients with endometrial cancer and patients with endometrial hyperplasia. It identified specific alterations of nosologic continuum of pathology and characterize areas of interest on the genome.


Clinical Trial Description

make a pangenomic investigation of genetic abnormalities in atypical endometrial hyperplasia and endometrial cancers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03338985
Study type Interventional
Source CHU de Reims
Contact Emilie RAIMOND
Phone 0326789598
Email eraimond@chu-reims.fr
Status Recruiting
Phase N/A
Start date October 16, 2017
Completion date April 16, 2020