Crohn Disease, Inflammatory Bowel Diseases, Ulcerative Colitis
Conditions
Brief summary
This is a prospective, non-interventional registry and biorepository for patients with IBD. Longitudinal follow-up data is collected from both patients and their treating gastroenterologist during routine clinical encounters. The biorepository will consist of prospective collection of blood samples, tissue samples, and fecal samples for research purposes, while the participants are undergoing a clinically-indicated procedure (i.e. venipuncture for routine tests, IV catheter placement, and/or endoscopy). Participants may choose to provide any or all of the aforementioned information and/or samples.
Interventions
OTHERNO INTERVENTION
THERE IS NO INTERVENTION TO THIS TRIAL. THIS IS A REGISTRY
Sponsors
University of Texas at Austin
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* Male or female, age 18 years or older * Willing and able to provide written consent for participation in the registry and biorepository * Patients with known or suspected inflammatory bowel disease
Exclusion criteria
* Patient is unable to comprehend and/or cooperate with study activities * Patient is too ill to provide consent * Coagulopathy that precludes safe biopsy of the bowel * Comorbidity that precludes safe participation in endoscopic procedures
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of patients with inflammatory bowel disease | 10 YEARS | Number of patients with Crohns, ulcerative colitis, and IBD undetermined |
Countries
United States
Contacts
Primary ContactBenjamin Chebaa, BA
Outcome results
None listed