Efficacy and Saffety of Oral Immunotherapy to Pistachio

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-01

Study Completion Date

2023-01-16

Brief Summary

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The objectives of this study are (i) to evaluate the efficacy of oral immunotherapy to pistachio by evaluating the daily oral tolerance of 2g pistachio, by evaluating the long-term tolerance of 15g pistachio (sustained unresponsiveness) and by decreasing pistachio-specific IgE, (ii) evaluating the efficacy of pistachio immunotherapy on cashew tolerance, (iii) and to evaluate the safety of pistachio immunotherapy.

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Detailed Description

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Conditions

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Allergy Food Allergy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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Food allergy

Oral immunotherapy to pistachio

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients under 18 years of age with a proven allergy to pistachio and followed in the pediatric allergology unit of the Nancy University Hospital.
* Patients who have received oral immunotherapy to pistachio for at least 18 months at 31/12/2022

Exclusion Criteria

* Patients who have received oral immunotherapy to pistachio for less than 18 months.
* Patients lost to follow-up for more than 2 years or last consultation dating from 2020 or earlier

Minimum Eligible Age

1 Year

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes