Actively Recruiting

Age: 4Years - 18Years
All Genders
ID06421415

Long Term Effect of Allergen Immunotherapy in Children with Allergy

Led by Odense University Hospital · Updated on 2025-07-10

100

Participants Needed

2

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to study the long-term effects of allergen immunotherapy in children with allergies. It focuses on children aged 5 to 18 years undergoing treatment with subcutaneous or sublingual immunotherapy for allergens such as grass pollen, birch, house dust mites, or venom. The study is observational and takes place in a real-life setting to understand lasting outcomes after immunotherapy. Children treated at Hans Christian Andersen Children's Hospital, Odense University Hospital, will be followed. Before starting immunotherapy, consent will be obtained to register data and send questionnaires 5 and 10 years after treatment ends. Baseline data includes symptoms, medication use, blood tests, and skin prick results. During treatment, yearly monitoring of symptoms, medication, lung function, and side effects will occur. Participants will receive questionnaires 5 and 10 years after treatment to assess allergy and asthma symptoms and medication use. The main outcome measured is the effect of immunotherapy 5 years after treatment, with a secondary outcome at 10 years. This long-term follow-up helps researchers understand how immunotherapy impacts children’s allergies over time.

CONDITIONS

Brief Title

Long Term Effect of AIT in Children

Who Can Participate

Age: 4Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 5 to 18 years treated with allergen immunotherapy at Hans Christian Andersen Children's Hospital, Odense University Hospital
Not Eligible

You will not qualify if you...

  • Received less than 12 months of allergen immunotherapy treatment

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - At least 12 months

Participants receive allergen immunotherapy as part of their usual care while the study observes the long-term effects of the treatment.

Annual visits during treatment

Long-term Monitoring

Duration - 10 years after treatment ends

Participants complete questionnaires 5 and 10 years after the end of treatment to assess allergy symptoms, medication use, and asthma symptoms.

2 follow-up questionnaire contacts (at 5 and 10 years post-treatment)

Trial Site Locations

Total: 2 locations

1

Hans Christian Andersen Children's Hospital

Odense, Odense C, Denmark, 5000

Actively Recruiting

2

Hans Christian Andersen Children's Hospital

Odense, Denmark, 5000

Actively Recruiting

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Research Team

J

Josefine Gradman, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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