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Environmental Peanut & tree nut elimination to enhance Oral immunotherapy in Children (EPOC): a randomized controlled trial

Environmental Peanut & tree nut elimination to enhance Oral immunotherapy in Children (EPOC): a randomized controlled trial - EPOC Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1041230036
Enrollment
40
Registered
2023-06-12
Start date
2023-06-12
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

IgE-mediated food allergy (peanut, tree- nut) food allergy, oral immunotherapy, environmental antigens, peanuts, tree nuts

Interventions

The environmental elimination group, as an intervention group, are instructed the removal of culprit foods from the household and the grandparents' house visited once a week or more until the end of t
N / A
environmental allergen elimination

Sponsors

Natsume Osamu
Lead Sponsor
Hayano Satoshi
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Pre-school children (under 6 years of age). 2. Those who avoid peanuts or tree nuts before starting oral immunotherapy. 3. Those who have had a positive result in an oral food challenge (OFC) for peanuts or tree nuts according to the PRACTALL criteria, with an amount of 0.1g to less than 3g. 4. Those who have had a positive result in food-specific IgE or SPT within the past 12 months. 5. Those whose legal guardians have provided written consent in this study.

Exclusion criteria

Exclusion criteria: 1. Not consuming the study food in either the cohabiting family or grandparents of the study subject. at the time of obtaining consent. 2. Poor control of atopic dermatitis or bronchial asthma. 3. Chronic urticaria. 4. Those judged ineligible by the responsible physician or participating physician at the study site due to severe illnesses or other reasons.

Design outcomes

Primary

MeasureTime frame
The single highest tolerated dose in the peanut/tree-nut OFC 24 months after the start of the trial (4-SU, four weeks sustained unresponsiveness)

Secondary

MeasureTime frame
1. The intergroup difference in the rate of change in single highest tolerated dose in the peanut/tree-nut OFC between before the start of the trial and 24 months after the start of the trial. 2. The intergroup difference in the proportion (efficacy rate) of those whose single highest tolerated dose in the peanut/tree nut OFC improved to more than 30 times the baseline before the start of the trial and 24 months after the start of the trial. 3. The intragroup differences in the before-and-after single highest tolerated dose in the peanut/tree nut OFC before the start of the trial and 24 months after the start of the trial. 4. The intragroup and intergroup differences in the rate of change of specific IgE and specific IgG4 levels, as well as the mean wheal size of skin prick tests (SPT) to the culprit foods, before the start of the trial and 12 and 24 months after the start of the trial. 5. Regarding the environmental antigen levels: 5-a. The correlation between the rate of change in environmental antigen levels and the single highest tolerated dose in the peanut/tree nut oral food challenge before the start of the trial and 24 months after the start of the trial. 5-b. The correlation between the mean environmental antigen levels during the trial period and the rate of change of specific IgE levels, IgG4 levels, and SPT mean wheal size before the start of the trial and 12 and 24 months after the start of the trial. 5-c. The intragroup and intergroup differences in the environmental antigen levels at the start of the study.

Contacts

Public ContactOsamu Natsume

Hamamatsu University School of Medicine

natsumeo@hama-med.ac.jp+81-53-435-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026