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ID00267501

Eosinophils and Inflammation, an Expanded Study

Led by Children's Hospital Medical Center, Cincinnati · Updated on 2025-09-17

5000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the underlying mechanisms of eosinophil growth, survival, migration, and function. This study aims to better understand the pathophysiology, clinical symptoms, and range of severity in diseases caused by eosinophilic inflammation in humans. It is an observational study sponsored by the Children's Hospital Medical Center, Cincinnati. Participants will not receive any treatment as part of this study since it is observational. The study involves collecting data and samples to analyze eosinophilic disorders and related conditions such as eosinophilic gastrointestinal disease, eosinophilic inflammatory disease, and food allergies. There are no specific intervention groups or treatments assigned. During the study, participants will provide informed consent, and if minors aged 11 or older, assent will also be obtained. The study includes individuals diagnosed with eosinophilic or food allergy conditions, their family members, or healthy controls. Researchers will collect and analyze clinical and biological data to better characterize these diseases. Participation involves observational assessments and sample collection with long-term follow-up possible, lasting until 2050.

CONDITIONS

Brief Title

Data and Sample Collection Study to Elucidate the Mechanisms of Eosinophilic Disorders

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent obtained from the patient or parent/guardian
  • Assent obtained from minors 11 years of age and older
  • Diagnosis of eosinophilic gastrointestinal disease, eosinophilic inflammatory disease, or food allergy, or being a family member or normal control
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Sample Collection

Duration - Ongoing during study participation

Participants provide biological samples to help elucidate mechanisms of eosinophilic disorders.

Long-term Monitoring

Duration - Up to study completion in 2050

Participants are observed over time to monitor disease status and progression.

Trial Site Locations

Total: 1 location

1

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, United States, 45229-3039

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Research Team

B

Bliss Magella

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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