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French Digestive Polyposis Cohorte Family Adenomatous Polyposis With APC and MYH Gene Mutations , Cowden's Disease With PTEN Gene Mutation, Peutz Jeghers Disease With STK 11 Gene Mutation ,juvénil Polyposis With SMAD 4 Gene Mutation , Serrated and Hyperplastic Polyposis

French Digestive Polyposis Cohorte

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01987518
Enrollment
350
Registered
2013-11-19
Start date
2011-01-31
Completion date
2020-08-31
Last updated
2018-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality of Life

Brief summary

French cohorte about polyposis digestive diseases

Detailed description

Family Adenomatous Polyposis APC and MYH Genes Peutz Jeghers Disease Cowden Disease Festooned polyposis Juvenile polyposis Hyperplastic polyposis

Interventions

OTHERProcedure surgery behavioral and genetic diagnosis

Observational Study

PROCEDUREquality of life after different type of surgery

Sponsors

Hôpital Edouard Herriot
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to 90 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
genetic diagnosis or over 50 polyps in the stomach in the duodenum or in the colon10 years

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026