Crohn's Disease and Colitis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
As a Case (person with IBD):
- People who have been diagnosed with confirmed inflammatory bowel disease (IBD), such as Crohn's disease or ulcerative colitis
- People whose IBD symptoms started at least 3 months ago
As a Control (comparison participant):
- People aged 18 or older who are a sibling, cousin, or neighbour of someone with IBD (note: people with IBD who are under 18 will not be included in the case-control part of the study)
- One sibling or cousin, and one neighbour, per person with IBD are needed as controls
Who may not be able to join:
Controls only (there are no exclusions listed for cases):
- People who are suspected of having inflammatory bowel disease
- People who have unexplained gut symptoms, including diarrhoea, vomiting, ongoing stomach pain, unexplained weight loss, blood in the stool, or a recent change in bowel habits
- People who have had gut surgery where the reason was never fully explained
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Leolin Katsidzira, MD, University of Zimbabwe
Phone: +263 77 2377 416
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Demographic and phenotypic features of inflammatory bowel disease
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.