About this trial
The goal of this observational study is to learn whether a rapid stool-based imaging test can help monitor inflammatory bowel disease (IBD) in children. The study will use a technology called differential mobility spectrometry (DMS) to analyze the molecular profile of stool samples. Researchers hope this method will provide a quick, non-invasive way to measure bowel inflammation and predict disease worsening.
The main questions it aims to answer are:
* Do children with IBD have different stool molecular profiles than children without IBD? * Can stool molecular profiles reflect how much inflammation is present in the bowel? * Can stool molecular profiles help predict disease relapse or the need for stronger treatment? * Can changes in stool molecular profiles show whether treatment is working?
Current methods used to monitor IBD have limitations. Blood tests, symptom scores, stool calprotectin tests, ultrasound, and endoscopy can help measure inflammation, but some tests are invasive, may not give immediate results, or may not accurately predict future disease activity. Researchers want to determine whether stool molecular profiling can provide additional information to support clinical care.
The study will include children younger than 18 years who are undergoing colonoscopy at Tampere University Hospital. Participants with IBD will be followed regularly for up to 5 years or until they transfer to adult care. Researchers will track disease activity, relapses, and treatment changes over time. Children without IBD will participate only at the baseline visit.
Participants with IBD will provide stool samples for stool molecular profiling and faecal calprotectin testing, and undergo routine assessments of disease activity, including symptom scores, blood tests, intestinal ultrasound, and elastography. Information from clinically indicated colonoscopies and tissue samples will be reviewed and compared to stool profiles. Attend follow-up visits will be performed approximately every 3 months for monitoring treatment response, relapses, and the need for treatment escalation. Researchers will compare stool molecular profiles between children with and without IBD. They will also compare patterns seen during remission and active disease and evaluate whether certain profiles are linked to treatment-resistant disease.
This study is expected to involve minimal risk because it mainly uses stool samples and clinical information collected during routine care. If successful, the findings could help develop a rapid and non-invasive tool that provides real-time information about bowel inflammation, reduces the need for invasive testing, and helps identify children at risk of relapse before symptoms worsen. This could support earlier and more personalized treatment decisions for children with IBD.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Scheduled for colonoscopy by pediatric gastroenterologist
Disqualifiers
None
Trial population
Children who are treated at the pediatric gastroenterology unit in Tampere University Hospital, have consented for the study, and are scheduled for colonoscopy
Trial design
Case-control
Prospective
Treatments tested in this trial
Differential Mobile Spectrometry analysis of the stool
Other interventionThe stool that is checked for faecal calprotectin will also be analysed using the DMS, which generates different ion spectra that will be referred as faecal molecular profile (FMP).
Treatment groups
Trial outcomes
Primary outcomes
Images of Fecal molecular profile (FMP) in children with and without IBD
Based on the DMS analysis of the stool, FMP and fecal calprotectin of children with IBD (both newly diagnosed and already treated) will be compared to those without IBD.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Tampere University Hospital
Lead sponsor
Olfactomics Oy
Collaborator
This trial is not recruiting at the moment. You can still explore other options: