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OpenTrials
Completed

NCT Number: NCT01172665

Celiac Disease Database

The focus of this study is to create a database containing information about patients with celiac disease. This database will allow us to examine clinical and epidemiologic features of the University of Chicago Medical Center patient population. We have the largest population of patients with celiac disease in the mid-West and as such this study using information gathered from our database can greatly contribute to our current understanding of this disease.

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Key information

Age range

0 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The University of Chicago Medical Center

Chicago, Illinois, 60637, United States

About this study

This database will allow us to examine clinical and epidemiologic features of the University of Chicago Medical Center patient population.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Must be a patient at The University of Chicago Medical Center
  • Clinical diagnosis of celiac disease or gluten sensitivity

Exclusion criteria

  • Currently being treated at a healthcare facility other than The University of Chicago Medical Center
  • Not diagnosed with celiac disease or gluten sensitivity

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Registry information

Official study title

University of Chicago Celiac Disease Database

Important dates

Study start
2008
Primary completion
2024
Study completion
2024
First posted
Jul 30, 2010
Registry last updated
May 16, 2024

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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