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Celiac DiseaseNCT01172665

Celiac Disease Database

An observational study of Celiac Disease, run by University of Chicago at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 0 to 70 years
Conditions the study is for
Celiac Disease
How many people
1,090 participants
Where
1 siteUnited States
Study dates
Sep 2008to 5 May 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 0 to 70 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Both pediatric and adult patients of The University of Chicago Medical Center who have been diagnosed with celiac disease or gluten sensitivity.

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

United States1 site
  • The University of Chicago Medical Center

    Chicago, Illinois, 60637

Other trials in United States

About this study

Official title: University of Chicago 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.

Read the detailed description

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

Conditions
Celiac Disease
Keywords
Celiac Disease
Medical subject headings
Celiac Disease

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Jul 2010 (estimated)
  2. Study startSep 2008
  3. Primary completion1 May 2024
  4. Study completion5 May 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Other
Enrolment
1,090 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01172665
Sponsor's protocol ID
16103A
Status last verified
May 2024
First submitted
28 Jul 2010
Last updated
16 May 2024
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Celiac Disease, run by University of Chicago at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 May 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 May 2024.

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