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Purpose

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

Eligibility

Eligible Ages
Between 18 Years and 100 Years
Eligible Sex
All
Accepts 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

Study Design

Phase
Study Type
Observational [Patient Registry]
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Inflammatory Bowel Disease any patient with IBD will be included in the registry
  • Other: NO INTERVENTION
    THERE IS NO INTERVENTION TO THIS TRIAL. THIS IS A REGISTRY

Recruiting Locations

Dell Medical School, UT Austin
Austin, Texas 78712
Contact:
Banjamin Chebaa, BA
512-495-5641
benjamin.chebaa@austin.utexas.edu

More Details

Status
Recruiting
Sponsor
University of Texas at Austin

Study Contact

Benjamin Chebaa, BA
5124955641
benjamin.chebaa@austin.utexas.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.