ID-in-FA: Improved Diagnostics in Food Allergy Study

Sponsor
Imperial College London (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT06097572
Collaborator
Royal College of Surgeons, Ireland (Other), University of Manchester (Other)
166
2
2
11.4
83
7.3

Study Details

Study Description

Brief Summary

The investigators will conduct low-dose intranasal allergen challenges on children and young people with an indeterminate diagnosis of food allergy to cow's milk or peanut. Blood samples will also be taken, for conventional blood allergy diagnostics (allergy-specific Immunoglobulin E) and mast cell activation test (MAT). The data will be used to determine the diagnostic accuracy of two complementary, novel approaches to diagnose food allergy, in a representative clinical cohort.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Intranasal food challenge
  • Diagnostic Test: Mast cell activation test
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
166 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Improved Diagnostics in Food Allergy (ID-in-FA) Study
Actual Study Start Date :
Oct 18, 2023
Anticipated Primary Completion Date :
Sep 30, 2024
Anticipated Study Completion Date :
Sep 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Peanut

Participants with possible allergy to peanut

Diagnostic Test: Intranasal food challenge
Subjects will undergo an incremental intranasal challenge to initially 0.9% NaCl saline solution, and then increasing doses of the food protein

Diagnostic Test: Mast cell activation test
Blood will be processed for mast cell activation as previously described (https://doi.org/10.1016/j.jaci.2018.01.043)

Experimental: Cow's Milk

Participants with possible allergy to cow's milk

Diagnostic Test: Intranasal food challenge
Subjects will undergo an incremental intranasal challenge to initially 0.9% NaCl saline solution, and then increasing doses of the food protein

Diagnostic Test: Mast cell activation test
Blood will be processed for mast cell activation as previously described (https://doi.org/10.1016/j.jaci.2018.01.043)

Outcome Measures

Primary Outcome Measures

  1. Test performance [1 day]

    Comparison of test performance characteristics (sensitivity, specificity, measured according to standard statistical methods) for each of the following diagnostic tests, compared to a formal oral food challenge (FC) as the reference standard: i. Intranasal FC (InFC) ii. Skin prick testing iii. Characterisation of serum-specific IgE to whole allergen, components and molecular components iv. Mast cell activation test (MAT) v. Basophil activation test (BAT) (peanut only)

Secondary Outcome Measures

  1. Adverse events [1 day]

    Number of participants who experience a non-allergic adverse event, and/or have symptoms of a systemic allergic reaction) associated with the intranasal food challenge.

Eligibility Criteria

Criteria

Ages Eligible for Study:
2 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • IgE-sensitisation to peanut, (hen's) egg or cow's milk, with indeterminate clinical (allergy) status, defined as IgE-sensitisation below 95% positive predictive value (PPV) for diagnosis for either allergen-specific IgE or SPT, using published cut-offs OR clinician suspicion of tolerance (on basis of clinical history) despite IgE sensitisation >95% PPV cut-offs.

  • Written informed consent from parent/guardian, with assent from children aged 6 years and above wherever possible. Participants aged over 16 years will need to provide their own informed consent.

Exclusion Criteria:
  • Acute illness or current unstable asthma, defined as:
  1. Febrile ≥38.0oC in last 72 hours

  2. Acute wheeze in last 72 hours requiring treatment

  3. Recent admission to hospital in preceding 2 weeks for acute asthma

  • Current medication
  1. Asthma reliever medication required in preceding 72 hours

  2. Recent administration of a medicine containing antihistamine within the last 3 days

  3. Current oral steroid for asthma exacerbation or course completed within last 2 weeks

  • Unwilling or unable to fulfil study requirements

Contacts and Locations

Locations

Site City State Country Postal Code
1 Prof Jonathan Hourihane Dublin Ireland
2 Imperial College Healthcare NHS Trust (St. Mary's Hospital) London United Kingdom

Sponsors and Collaborators

  • Imperial College London
  • Royal College of Surgeons, Ireland
  • University of Manchester

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Imperial College London
ClinicalTrials.gov Identifier:
NCT06097572
Other Study ID Numbers:
  • 22SM7832
  • 22/NW/0321
First Posted:
Oct 24, 2023
Last Update Posted:
Oct 24, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 24, 2023