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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01169194
Other study ID # NA_00041578
Secondary ID U01DK062431
Status Recruiting
Phase
First received
Last updated
Start date June 2003
Est. completion date August 2027

Study information

Verified date October 2023
Source Johns Hopkins University
Contact Lisa Datta, MS
Phone 410-502-0040
Email ibd@jhu.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators are doing the research to discover genes that cause Inflammatory Bowel Disease (IBD) specifically in the African American population. African Americans with or without Crohn's disease or ulcerative colitis are eligible to join. If you agree to join the study, the investigators will ask for information about your health. The investigators will also ask you to give us a blood sample so that they may discover the genes that cause IBD. The blood sample may be collected at Johns Hopkins or any local facility convenient to you.


Description:

This current protocol was established as part of an NIDDK initiative to further explore genetic factors associated with IBD. Specifically, the investigators are interested in identifying the genetic, environment and socio-economical components that contribute to the development of IBD in the African American population. IBD is believed to be caused by a combination of environmental and genetic factors. Genetic data will be examined alongside potential environmental factors such as smoking, medications, environmental exposures, and some dietary factors. Since IBD is known to predominantly affect Western, industrialized areas of the world, the investigators will also inquire about participants' socioeconomic background in hopes of identifying any previously unknown factors in the AA population that may increase the risk of IBD. These potential environmental factors will be important in association analyses using covariates as these factors can obscure potential associations or interact with genetic factors and thus contribute to genetic associations. The investigators will also obtain information as to ancestry of parents and grandparents as to best match cases with unrelated controls of similar ancestry (e.g., Caribbean, recent European or recent African ancestry could cause genetic mismatch of a case and control). At the same time, the investigators will also collect similar information (smoking, medications, environmental exposures and dietary factors) from non-African Americans for the purpose of making direct comparisons for these parameters between the different racial groups to assess the contribution of non-genetic factors for susceptibility to the development of IBD. This study calls for recruiting AA patients and ethnically matched controls (friend or spouse). These persons will provide us with a blood sample and with information requested on a questionnaire asking the following: clinical course and history of their IBD or their general health, smoking history, socioeconomic variables and specific dietary factors known in some populations to be related to IBD etiology. Access to medical records will be used to confirm diagnoses. The clinical characteristics of IBD obtained from medical records will be summarized in a phenotyping form using a standardized NIDDK IBDGC Phenotyping Operations Manual. Controls will be asked health history to identify potentially unrecognized IBD. DNA and other biospecimens will be purified from blood. Samples and data will also be shared with the NIDDK IBDGC for use in IBDGC research projects and will be processed and maintained at NIDDK repositories.


Recruitment information / eligibility

Status Recruiting
Enrollment 2400
Est. completion date August 2027
Est. primary completion date August 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years and older
Eligibility Inclusion Criteria: 1. African Americans with a confirmed diagnosis of Inflammatory Bowel Disease (IBD) 2. African Americans without a diagnosis of IBD and without a family history of IBD for comparison purposes Exclusion Criteria: Patients whose IBD cannot be confirmed

Study Design


Locations

Country Name City State
United States Johns Hopkins University School of Medicine Baltimore Maryland
United States University of Alabama at Birmingham Birmingham Alabama
United States University of Chicago Chicago Illinois
United States Baylor College of Medicine Houston Texas
United States Robert Wood Johnson Medical School New Brunswick New Jersey
United States Weill Cornell Medical College New York New York

Sponsors (7)

Lead Sponsor Collaborator
Johns Hopkins University Baylor College of Medicine, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH), Rutgers University, University of Alabama at Birmingham, University of Chicago

Country where clinical trial is conducted

United States, 

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