Eosinophilic Gastroenteritis

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Review clinical trials related to Eosinophilic Gastroenteritis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Eosinophilic Gastrointestinal Disorders Registry

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

Participants needed: 500
Trial details
Age: 1-25Biological sex: AllType: ObservationalSponsor: Ann & Robert H Lurie Children's Hospital of ChicagoUpdated: Mar 18, 2026Locations: 1Duration: 5 Years
Eligibility criteria

Patients with an established diagnosis of an EGID, based on pathology findings f... [+1]

Patients who do not consent to participate

Status: Recruiting

OMEGA: Outcome Measures in Eosinophilic Gastrointestinal Disorders Across the Ages

The purpose of this observational study is to find the best measures to define how well a person with eosinophilic disorder is doing. People with EoE, EoG, EoN and EoC normally undergo endoscopy and/or colonoscopy where cells are collected for microscopic analysis. Treatments are then decided based on how the cells look. We are aiming to compare different tissue components such as inflammatory cell types with clinical symptoms. We want to see if scores on standard questionnaires can give us an idea how well the person is doing.

Participants needed: 1,350
Trial details
Age: 3+Biological sex: AllType: ObservationalSponsor: Children's Hospital Medical Center, CincinnatiUpdated: Sep 12, 2025Locations: 19
Eligibility criteria

Males or females 3 years of age and older

History of intestinal surgery other than G tube placement [+3]

Status: Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.

Participants needed: 20,000
Trial details
Biological sex: AllType: ObservationalSponsor: Sanford HealthUpdated: May 29, 2025Locations: 2Duration: 100 Years
Eligibility criteria

Diagnosis of a rare disease, a disease of unknown prevalence, undiagnosed or an...

Diagnosis of a disease which is not rare