A Registry for Patients With Food Allergy

  • End date
    Aug 27, 2023
  • participants needed
  • sponsor
    Food Allergy Research & Education
Updated on 27 January 2021
Patient Registry Coordinator
Primary Contact
NorthShore University HealthSystem (7.7 mi away) Contact
+17 other location


The FARE Patient Registry will serve as a prospective, observational food allergy reporting system that stores detailed health and other basic information about patients' real-world experiences with food allergies, to encourage open sharing of de-identified data and participation in clinical trials. The FARE Patient Registry intends to make and support scientific discoveries by enabling the food allergy community to participate directly in research.

Condition Food Allergy, Eosinophilic esophagitis, anaphylaxis, Food Intolerance, Food Allergy in Infants, Food Sensitivity, anaphylactic shock, anaphylactic reaction, anaphylactic reactions, food intolerances, food allergies
Clinical Study IdentifierNCT04653324
SponsorFood Allergy Research & Education
Last Modified on27 January 2021


Yes No Not Sure

Inclusion Criteria

Individuals with a suspected or diagnosed food allergy

Exclusion Criteria

Individuals without food allergy
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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