Prevalence and Description of FIRE (Food Induced Immediate Response of the Esophagus) in the Pediatric Population With Eosinophilic Esophagitis
FIREO
2 other identifiers
observational
40
1 country
2
Brief Summary
A new clinical entity of eosinophilic esophagitis, Food Induced Immediate Response of the Esophagus or FIRE, has been described since 2020. Diagnostic criteria are not clearly established. Specific questioning is necessary for differential diagnosis, such as the oro-pharyngeal syndrome notably described in pollinics, or a mechanical blockage strictly speaking linked to esophagitis. The aim is to obtain epidemiological data on this entity.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jul 2025
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 14, 2025
CompletedFirst Posted
Study publicly available on registry
May 14, 2025
CompletedStudy Start
First participant enrolled
July 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedDecember 24, 2025
October 1, 2025
10 months
March 14, 2025
December 23, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
diagnosis of FIRE syndrome
symptoms such as pain, pressure, choking or narrowing, in the oesophagus or retrosternum, within 10 minutes of ingestion, lasting a maximum of 120 minutes, when a specific food is ingested
day 1
Study Arms (1)
eosinophilic esophagitis
questionnary
Eligibility Criteria
Patient follow-up in the allergology unit of Angers University Hospital
You may qualify if:
- Follow-up in the allergology unit of Angers University Hospital for eosinophilic esophagitis
You may not qualify if:
- Patients or legal representative with severe communication or language comprehension difficulties
- Patients or legal representatives objecting to study participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
HOPPE Anne
Angers, France
CHU Lille
Lille, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anne HOPPE
University Hospital of Angers
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 14, 2025
First Posted
May 14, 2025
Study Start
July 1, 2025
Primary Completion
May 1, 2026
Study Completion
May 1, 2026
Last Updated
December 24, 2025
Record last verified: 2025-10