# 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

> **NCT01987518** · — · UNKNOWN · sponsor: **Hôpital Edouard Herriot** · enrollment: 350 (estimated)

## Conditions studied

- Quality of Life

## Interventions

- **OTHER:** Procedure surgery behavioral and genetic diagnosis
- **PROCEDURE:** quality of life after different type of surgery

## Key facts

- **NCT ID:** NCT01987518
- **Lead sponsor:** Hôpital Edouard Herriot
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2011-01
- **Primary completion:** 2014-08
- **Final completion:** 2020-08
- **Target enrollment:** 350 (ESTIMATED)
- **Last updated:** 2018-02-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01987518

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01987518, "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". Retrieved via AI Analytics 2026-05-29 from https://api.ai-analytics.org/clinical/NCT01987518. Licensed CC0.

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