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French Digestive Polyposis Cohorte
study id #: NCT01987518
condition: Quality of Life
status: Recruiting
purpose:French cohorte about polyposis digestive diseases
intervention:
Other: Procedure surgery behavioral and genetic diagnosis
Procedure: quality of life after different type of surgery
start date: January 2011
estimated completion: August 2020
last updated: February 28, 2018
phase of development: Not Available
size / enrollment: 350
study design:
Observational Model: Cohort
Time Perspective: Retrospective
study description:
Family Adenomatous Polyposis APC and MYH Genes Peutz Jeghers Disease Cowden Disease Festooned polyposis Juvenile polyposis Hyperplastic polyposis
primary outcomes:
- genetic diagnosis or over 50 polyps in the stomach in the duodenum or in the colon [ Time Frame: 10 years ] [ Designated as safety issue: Yes ]
inclusion criteria:
APC Gene mutation
MYH Homozygote mutation
COWDEN Disease with PTEN gene mutation
Peutz Jeghers Disease with STK 11 gene mutation
Juvenile polyposis with SMAD 4 gene mutation
exclusion criteria:
heterozygote MYH Gene Mutation
sponsor: Hôpital Edouard Herriot
contacts:
Saurin Jean Christophe, msd
(33)0472117572
jean-christophe.saurin@chu-lyon.fr
Vinet Olivier, CRA
(33)0472110370
olivier.vinet@chu-lyon.fr
investigators: Jean Christophe Saurin, MSD
locations: France
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