MICROPRUNG : Intestinal Microbiota Analysis in Patients With or Without Hirschsprung's Associated EnteroColitis

NCT ID: NCT02857205

Last Updated: 2018-09-13

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

118 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-06-30

Study Completion Date

2018-09-30

Brief Summary

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Hirschsprung disease is a congenital abnormality due to the lack of migration of neural crest cells in myenteric and submucosal plexi of the bowel wall. The consequence is the absence of parasympathetic control of the distal bowel from the anal sphincter to various levels. The most common type of Hirschsprung disease alters the rectosigmoid (80%). The incidence is around 1/5000 live births. This anomaly requires a surgical ablation of the aganglionic segment.

Regardless of the surgical complications, patients with Hirschsprung disease are exposed to the risk of Hirschsprung Associated EnteroColitis (HAEC). This variable risk, 4-54%, is responsible to a major part of Hirschsprung disease morbimortality. Its onset is more frequent during the first two years of life and then decrease with age.

Its pathogenesis remains unclear but could be due to intestinal homeostasis breakdown that involves microbiota, intestinal barrier, immune system and enteric nervous system. This breakdown of the mutual benefit relation due to microbiota or bowel anomaly is known to be responsible of Crohn's disease onset. Some studies emphasize the role of microbiota in the pathogenesis of HAEC, but the techniques or the methodology with small numbers of patients limit any conclusion or clinical use.

The study hypothesizes microbiota is a major factor in HAEC onset and in their functional bowel problems. Considering HAEC is more frequent the first two years, it's thought that intestinal microbiota changes with time in those patients. This project is innovative because it will use high throughput sequencing methods and analysis for microbiome analysis on fecal samples from a multicenter cohort of patients at various ages.

Multicentre transversal study.

This study has the potential to significantly modify clinical practice for Hirschsprung disease patients: a better care for HAEC and functional troubles thanks to a better understanding of their microbiota, targetted antibiotic treatment for HAEC, prophylactic treatment of patients at high risk of HAEC.

Detailed Description

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Primary objective :

Characterize intestinal microbiota in patients with or without HAEC.

Secondary objectives :

* Look for a difference in microbiota composition between patients with or without HAEC ;
* Study the evolution with age of the microbiota in Hirschsprung disease patients ;
* Study predominant taxonomic classification elements in both groups.

Conditions

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Hirschsprung Disease

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Fecal samples

High throughput sequencing methods and analysis for microbiome analysis on fecal samples from a multicenter cohort of patients at various ages.

Group Type OTHER

Fecal samples

Intervention Type OTHER

High throughput sequencing methods and analysis for microbiome analysis on fecal samples from a multicenter cohort of patients at various ages.

Interventions

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Fecal samples

High throughput sequencing methods and analysis for microbiome analysis on fecal samples from a multicenter cohort of patients at various ages.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients from 0 to 16 years ;
* With rectosigmoid Hirschsprung's disease confirmed by rectal biopsies and at surgery;
* Already operated on, whatever the surgical technique was ;
* With a health care insurance;
* Clear information and signed consent form

Exclusion Criteria

* Long segment Hirschsprung disease ;
* Syndromic Hirschsprung disease ;
* Down syndrome.
Maximum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rennes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Alexis ARNAUD, MD

Role: PRINCIPAL_INVESTIGATOR

Rennes University Hospital

Locations

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Angers University Hospital

Angers, , France

Site Status

Brest University Hospital

Brest, , France

Site Status

Caen Univeristy Hospital

Caen, , France

Site Status

Nantes University Hospital

Nantes, , France

Site Status

Poitiers University Hospital

Poitiers, , France

Site Status

Rennes University Hospital

Rennes, , France

Site Status

Tours University Hospital

Tours, , France

Site Status

Countries

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France

References

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Arnaud AP, Cousin I, Schmitt F, Petit T, Parmentier B, Levard G, Podevin G, Guinot A, DeNapoli S, Hervieux E, Flaum V, De Vries P, Randuineau G, David-Le Gall S, Buffet-Bataillon S, Boudry G. Different Fecal Microbiota in Hirschsprung's Patients With and Without Associated Enterocolitis. Front Microbiol. 2022 Jun 30;13:904758. doi: 10.3389/fmicb.2022.904758. eCollection 2022.

Reference Type DERIVED
PMID: 35847080 (View on PubMed)

Other Identifiers

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2015-A01317-42

Identifier Type: OTHER

Identifier Source: secondary_id

35RC15_9873_MICROPRUNG

Identifier Type: -

Identifier Source: org_study_id

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