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OpenTrials
Enrolling by Invitation

NCT Number: NCT03756649

Mayo Clinic IBD Biobank

Researchers are collecting and storing blood, stool, and urine samples and medical information to better understand Inflammatory Bowel Disease (IBD) to improve disease outcome.

Enrolling by Invitation

Interested in participating?

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Mayo Clinic

Rochester, Minnesota, 55905, United States

About this study

Subjects will be sent a letter detailing the proposed biobank and soliciting enrollment. Following the informed consent process, subjects will provide a blood sample (50 ml), urine sample (50 ml), and stool. The blood and urine samples will either be collected at the one of the Mayo Clinic outpatient laboratories or by a mail-out kit. Subjects will be asked to complete a questionnaire and 24-hour food recall questionnaire (completed online).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with inflammatory bowel disease (IBD) who are between the ages of 18 and 85 at time of study enrollment.
  • The diagnosis of IBD will be based on the standard IBD criteria including biochemical and colonoscopy screening.
  • Women with inflammatory bowel disease of childbearing potential and pregnant women will be offered enrollment because there is no risk to an unborn child in this investigation.
  • Patients between the ages of 18 and 85 without history of IBD or colon cancer.

Exclusion criteria

  • Patients with known liver disease.
  • Patients unable to provide informed consent.
  • Prisoners and institutionalized individuals.
  • Patients with a history of colorectal cancer.

Treatment and study plan

Blood draw

Procedure

50 ml will be collected

Urine collection

Procedure

50 ml will be collected

Stool Collection

Procedure

Three 25 ml tubes will be collected

Primary outcomes

  1. Study Participants

    Time frame: 50 years

    Total number of participants in the study

Secondary outcomes

  1. Urine Collection

    Time frame: 50 years

    Total number of urine samples collected

  2. Blood Collection

    Time frame: 50 years

    Total number of blood samples collected

  3. Stool Collection

    Time frame: 50 years

    Total number of stool samples collected

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Important dates

Study start
2018
Primary completion
2065
Study completion
2065
First posted
Nov 28, 2018
Registry last updated
Feb 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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