Health TrialsbyHealthPanel

Observatory of the Lille Paediatric Allergy Unit

ConditionsChild AllergyIgE-Mediated Allergic ProcessFood Allergy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 16
SponsorLille Catholic University

About this trial

The goal of this study is to set up a paediatric observatory within the allergology department of The saint Vincent Hospital, Lille. The study aims to:

• Collect exhaustive prospective data from patients eligible for oral immunotherapy.

This prospective observatory will enable statistical analyses to be carried out on common food allergens such as hazelnut, cashew nut, pistachio and others.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patient under 15 years and 9 months,

positive diagnosis of food allergy (positive food challenge test or "highly probable allergy", defined by a convincing history, a positive prick test and IgE > 0.35 kUA/L),

eligible for oral food challenge

accepting the following allergens : hazelnut, walnut, pistachio, cashew, peanut, cow's milk, wheat, egg, sesame, celery, fenugreek, pea, lentils or others

Disqualifiers

Opposition

Already received oral challenge for the same allergen.

Trial population

All eligible patients consulting at the allergology service of the Saint Vincent Hospital, Lille, France will be informed and included, unless they object.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Oral immunotherapy

    Other intervention

    Clinical Follow up

Treatment groups

1,000 Participants
are divided into 3 treatment groups
Group A: Group 11 intervention
Group B: Group 21 intervention
Group C: Group 31 intervention

Trial outcomes

Primary outcomes

1

Age

For each patient, and for each visit during the treatment period the collection of anthropometric, sociodemographic and medical data relating to oral food challenge will be done

Time frame
at inclusion
2

Sex

For each patient, and for each visit during the treatment period the collection of anthropometric, sociodemographic and medical data relating to oral food challenge will be done

Time frame
at inclusion
3

Oral immunotherapies followed before inclusion

For each patient, and for each visit during the treatment period the collection of anthropometric, sociodemographic and medical data relating to oral food challenge will be done

Time frame
at inclusion
4

Determination of comorbidities

For each patient, and for each visit during the treatment period the collection of anthropometric, sociodemographic and medical data relating to oral food challenge will be done

Time frame
at inclusion

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Lille Catholic University

Lead sponsor

Source ClinicalTrials.gov
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