About this trial
Objective:
To use clinical, genetic and genome analysis to better understand and define the genetic and environmental factors that contribute to IBD within affected populations.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Subjects: diagnosed with Inflammatory Bowel Disease (Crohn's disease, ulcerative colitis, IBD-undetermined)
Available medical records to confirm IBD diagnosis (Crohn's disease, Ulcerative colitis, IBD undetermined (IBD-U))
Healthy controls: no personal history of IBD, no family history of IBD, no history of unexplained chronic diarrhea/blood in stool/anemia/abdominal pain/weight loss
Any age
Disqualifiers
None
Trial population
IBD or Healthy controls (non-IBD)
Trial design
Case-control
Prospective
Treatments tested in this trial
Blood or saliva sample collection
GeneticBlood or saliva sample \& clinical data collection
Treatment groups
Trial outcomes
Primary outcomes
Genomics studies across populations
Whole Exome Sequencing (+/- other sequencing) is planned
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Mount Sinai Hospital, Canada
Lead sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborator