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
NCT ID: NCT01987518
Last Updated: 2018-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
350 participants
OBSERVATIONAL
2011-01-31
2020-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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digestive polyposis
Family adenomatous polyposis (APC or MYH genes) Peutz Jeghers Disease Cowden Disease Festooned Polyposis Juvenile Polyposis Hyperplastic Polyposis
Procedure surgery behavioral and genetic diagnosis
Observational Study
quality of life after different type of surgery
Interventions
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Procedure surgery behavioral and genetic diagnosis
Observational Study
quality of life after different type of surgery
Eligibility Criteria
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Inclusion Criteria
* 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
12 Years
90 Years
ALL
No
Sponsors
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Hôpital Edouard Herriot
OTHER
Responsible Party
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Jean Christophe Saurin
Principal Investigator
Principal Investigators
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jean christophe saurin, msd
Role: PRINCIPAL_INVESTIGATOR
HEH Hospital
Locations
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Hopital Edouard Herriot
Lyon, Auvergne-Rhône-Alpes, France
Countries
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Facility Contacts
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Other Identifiers
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SISRA
Identifier Type: OTHER
Identifier Source: secondary_id
Peps Data Base
Identifier Type: -
Identifier Source: org_study_id
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