Observational Study of IgE-Mediated Leguminous Allergies in a Pediatric Population
Condition(s) studied
Study summary
Prospective, monocentric, observational study with standard care follow-up during 5 years or until the patient reaches the age of 18.
The aim of this study is to prospectively and comprehensively assess the characteristics of patients aged 6 months to 17 years with leguminous allergy (excluding peanut) and their reactions to leguminous, including both medical history and prospective follow-up for 5 years from inclusion, or until the age of 18. The study aims to improve the understanding of these allergies, provide epidemiological data, and optimize diagnostic and clinical management. A biobank will also be established, with plasma (one whole blood sample collected at the inclusion) in order to validate future diagnostic tests.
Eligibility
Primary outcome measure(s)
- Prospectively study, among the leguminous, the type of leguminous (excluding peanut) responsible for the allergy. — Baseline (Inclusion) 1 Year from the Inclusion 5 years from the inclusion, or until the age of 18
The primary endpoint will be the number of allergy diagnoses for each type of leguminous (excluding peanut), among : * Green peas * Split peas (dried green peas) * Yellow or blond dried peas * Chickpeas * Green, red, or blond lentils * Green, Kidney, White or Mung beans * Soybean * Lupin * Fenugreek * Fava bean (broad bean) * Beluga lentils * Black-eyed peas (cowpeas), adzuki beans,and urad beans * Alfalfa
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU Lille | Lille | France |
More University Hospital, Lille trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07811141 on ClinicalTrials.gov ↗ ← All trials in France