Actively Recruiting

Age: 1Year - 25Years
All Genders
NCT05199532

Eosinophilic Gastrointestinal Disorders Registry

Led by Ann & Robert H Lurie Children's Hospital of Chicago · Updated on 2026-03-18

500

Participants Needed

1

Research Sites

780 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to learn more about Eosinophilic Gastrointestinal Disorders (EGIDs). With this registry we hope to find out more about the symptoms that patients have during their treatment, the quality of life they have with the diagnosis, what the disease looks like throughout the different treatment methods, and if there is a connection between EGIDs and connective tissue disorders. The goal of this study is to be able to better understand EGIDs and use information gained from all the information collected on this study for more precise treatments in the future. We want to create a large collection of samples, called a biorepository, to learn the most about EGIDs as possible. When the samples are collected, which will occur at procedures directed by your child's doctor as part of their standard of care, they will be stored for an unlimited amount of time to perform experiments on these samples and to gather information about EGIDs

CONDITIONS

Official Title

Eosinophilic Gastrointestinal Disorders Registry

Who Can Participate

Age: 1Year - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with an established diagnosis of an EGID based on biopsy results from endoscopy or colonoscopy
  • Patients suspected of having an EGID and undergoing endoscopic evaluation for further assessment
Not Eligible

You will not qualify if you...

  • Patients who do not consent to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ann & Robert H Lurie Children's Hospital of Chicago

Chicago, Illinois, United States, 60611

Actively Recruiting

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Research Team

A

Angela Anthony

CONTACT

M

Mary Riordan

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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