MOlecular BIomarkers and Adherent and Invasive Escherichia Coli (AIEC) Detection Study In Crohn's Disease Patients

Crohn's Disease Clinical Trial

— MOBIDIC  

Official title:

MOlecular BIomarkers and Adherent and Invasive Escherichia Coli (AIEC) Detection Study In Crohn's Disease Patients (MOBIDIC)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02882841
• Other study ID #: IBD210
• Status: Terminated
• Phase: N/A
• Start date: September 2016
• Est. completion date: December 2017

Study information

• Verified date: April 2018
• Source: Enterome
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is a multicenter, international descriptive study with a bio-collection in 300 evaluable Crohn's disease patients to be processed after usual biological tests via bioinformatics tools.

At this time, this study has no impact neither on treatment nor on disease diagnostic, these will be based on usual medical practices and is no investigational product associated with the conduct of this study.

Description:

350 Crohn's disease patients will be included in the study, targeting 300 evaluable patients. An interim analysis will be performed after 50% of the evaluable patients are recruited.

The primary objective is to evaluate the relation between non-invasive biomarkers (host immunological variables and metagenomic analysis in stools) and AIEC detection in biopsies taken during an endoscopy, in order to develop a predictive algorithm of AIEC carriage.

The secondary objectives are:

• Validation of the AIEC detection algorithm using qPCR technology.

• Assessment of the correlation between the presence of AIEC and the endoscopic and clinical evaluations of the disease (CDEIS, SES-CD, Harvey-Bradshaw Index and Crohn's Disease Activity Index).

• Development and validation of a non-invasive qPCR based diagnostic of Mucosal Healing in CD patients.

• Collection of biological samples associated with all clinical and biological data from CD patients.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 143
• Est. completion date: December 2017
• Est. primary completion date: December 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Male or female between 18 and 75 years of age, inclusive;

• With a diagnosis of ileal or ileo-colonic Crohn's disease for a minimum of 3 months prior to inclusion;

• An ileocolonoscopy scheduled prior to study inclusion;

• Agreeing to participate and to sign an informed consent form;

• Able to perform stool collection, at home, according to protocol;

• Covered by Health Insurance System and/or in compliance with the recommendations of National Law in force relating to biomedical research.

Exclusion Criteria:

• Colonic Crohn's disease of L2 phenotype based on Montreal classification;

• Extensive small bowel resection (> 100 cm) or short bowel syndrome

• Bowel strictures/stenosis contraindicating ilecolonoscopy;

• Currently with an ostomy or an ileoanal pouch;

• Currently receiving total parenteral nutrition;

• Bowel preparation received in the previous 3 months;

• An increased risk of hemorrhage (patients with anticoagulant/antiplatelet therapy)

• History of intestinal carcinoma and colorectal cancer;

• History or presence of alcohol or substance abuse;

• History of chronic uncontrolled disorders;

• Current participation in an investigational product trial;

• Less than 4 weeks since last participation in a clinical trial;

• Subject inapt or unwilling to participate to the study;

• Pregnant or breastfeeding mother;

• Patient under guardianship.

Related Conditions & MeSH terms

• Crohn Disease
• Crohn's Disease

Intervention

Other:
• Biopsies, stool and blood collection

Locations

Country	Name	City	State
France	Hôpital Saint-Antoine	Paris
United Kingdom	Guy's and St Thomas' NHS Foundation Trust	London
United States	Children's Hospital Boston	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Enterome	Eurofins Optimed

Countries where clinical trial is conducted

United States,  France,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary evaluation criterion is the correlation between the detection of AIEC using a non-invasive stool based algorithm and the detection of AIEC using an ileal biopsy taken during an endoscopy.		6-12 months between inclusion and analysis