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Clinical Trials in Canada / NCT06722456
Enrolling by invitation Observational

Assessment of Non-invasive Tools for Detecting Active Inflammatory Bowel Disease

NCT06722456 · tracked via the Priya Life Science Canada tracker
Sponsor
Jean-François Beaulieu
Phase
Observational
Started
2024-05-30
Last updated
2024-12-09

Condition(s) studied

Inflammatory Bowel Disease (IBD)Crohn Disease (CD)Ulcerative Colitis (UC)

Investigational drug(s) / intervention(s)

Analysis of protein signatures in stool samples

Analysis of protein signatures in stool samples: Stool protein signatures are to be established in parallel to standard clinical evaluation of the intestinal inflammatory activity.

Study summary

Part of the success of the treatment of people living with inflammatory bowel diseases (IBD) depends on the information that the doctor can obtain from the different clinical tests. Some of these tests are invasive such as the colonoscopy but other such the fecal calprotectin test, which measures intestinal inflammation, are non-invasive and useful to evaluate the success of the treatments. Unfortunately, the results from the non-invasive tests are not always clear and need to be complete with invasive tests for the right diagnosis.

The aim of this research is to test new stool markers for assisting the gastroenterologist to diagnose inflammatory bowel conditions including Crohn's disease (CD) and ulcerative colitis (UC) and to carefully monitoring the effects of medications on remission. We are using applications based on the use of mass spectrometry for identifying the proteins that are released by the host in the stools. We have identified more than 400 proteins in total. Based on informatics, we have been able to produce lists of unique stool proteins that can rapidly inform the doctor if the person has an IBD, whether it is a CD or an UC and, more importantly for the treatment, if the IBD is active or in remission.

The purpose of this study is to validate these protein markers in a blind test, where the real diagnosis will only be revealed after the analysis of the samples.

This study will bring a new power tool to assist the gastroenterologist in the treatment of people living with IBD.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Be affected with one of the two main inflammatory bowel diseases (Crohn's disease of ulcerative colitis). * Be invited to participate on the base of a routine follow up by their gastroenterologist. * Be scheduled for a calprotectin test and a colonoscopy. * Accept to participate and provide an extra stool sample for analysis. Exclusion Criteria: * Having no history of inflammatory bowel disease. * Be affected with an history of gastrointestinal disease other than Crohn disease or ulcerative colitis.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre de recherche of the CIUSSS de l'Estrie-CHUS Sherbrooke Quebec

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06722456 on ClinicalTrials.gov ↗ ← All trials in Canada