Actively Recruiting
Registry and Biorepository for IBD in Central Texas
Led by University of Texas at Austin · Updated on 2021-05-18
1000
Participants Needed
1
Research Sites
500 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Registry and Biorepository for IBD in Central Texas
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- Unable to comprehend and/or cooperate with study activities
- Too ill to provide consent
- Coagulopathy that prevents safe biopsy of the bowel
- Comorbidity that prevents safe participation in endoscopic procedures
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Dell Medical School, UT Austin
Austin, Texas, United States, 78712
Actively Recruiting
Research Team
B
Benjamin Chebaa, BA
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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