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.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Create a registry to characterize the extent of food allergy, its etiology and other factors that contribute to disease development.
Timeframe: 2023
Patient Registry Coordinator