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AsthmaFinnATOPYNCT06330974

Allergy, Asthma, and Atopic Eczema in Finland

An observational study of Asthma and Asthma in Children, run by Tampere University at 1 site in Finland.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

The summary is available at --> https://www.finnatopy.fi/summary Read more about this study

Who is it for?
Any age
Conditions the study is for
Asthma, Asthma in Children, Allergy
How many people
1,200,000 participants
Where
1 siteFinland
Study dates
1 Dec 2026to Dec 2034
How long will I take part?
7 Years
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: https://www.finnatopy.fi/methods

Inclusion/Exclusion Criteria ---> https://www.finnatopy.fi/methods

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Péter Csonka, MD, PhD contact

+358503661103

peter.csonka@tuni.fi

Finland1 site
  • Tampere University

    Tampere

Other trials in Finland

About this study

Official title: Allergy, Asthma, and Atopic Eczema in Finland - A Nationwide Study on Prevalence, Comorbidities, Treatment and Economic Burden

The summary is available at --> https://www.finnatopy.fi/summary

Read the detailed description

Aims and objectives ---> https://www.finnatopy.fi/aims-and-objectives Methods ---> https://www.finnatopy.fi/methods

Being tested
No intervention, No Intervention: Observational Cohort
Medical subject headings
Asthma, Hypersensitivity, Rhinitis, Allergic, Dermatitis, Atopic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No interventionOther

    No intervention

  • No Intervention: Observational CohortOther

    No intervention

Study groups in NCT06330974
Study groupRoleWhat they receive
AtopicPatientes with any atopic condition (g.e., asthma, atopic dermatitis, IgE-mediateid allergy)
Receives: Other: No intervention; Other: No Intervention: Observational Cohort
Control group - migranePatients with migrane
Receives: Other: No intervention; Other: No Intervention: Observational Cohort
Control group - celiac diseasePatients with celiac disease
Receives: Other: No intervention; Other: No Intervention: Observational Cohort
Control group - UTIPatients with urinary tract infection
Receives: Other: No intervention; Other: No Intervention: Observational Cohort
Control group - LRTIPatients with lower respiratory tract infection
Receives: Other: No intervention; Other: No Intervention: Observational Cohort
Control group - bronchitisPatients with acute bronchitis
Receives: Other: No intervention; Other: No Intervention: Observational Cohort

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Epidemiology of atopic diseases and allergic sensitization profiles in Finland

    Incidence and prevalence of asthma, specific IgE sensitization, atopic dermatitis, allergic rhinitis

    Measured: 7 years

  2. Burden of atopic diseases (allergies, asthma, and atopic eczema) as well as comorbidities in Finland

    Morbidity, sick leaves, medication use, costs and expences

    Measured: 7 years

  3. Evaluate and improve the current use of diagnostic tests for atopic diseases

    Diagnostic practices, tests for allergic sensitization, lung function tests, and other laboratory measures.

    Measured: 7 years

  4. Use and effectiveness of allergen immunotherapy in real world setting

    Real world evidence data using specific cohorts

    Measured: 7 years

  5. Direct and indirect costs related to atopic diseases and comorbidities

    All costs, including sick leaves, absenteeism, laboratory costs, other diagnisteic tests, etc.

    Measured: 7 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Mar 2024
  2. Study start1 Dec 2026 (estimated)
  3. Primary completionDec 2032 (estimated)
  4. Study completionDec 2034 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
1,200,000 participants (estimated)
Target duration
7 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT06330974
Sponsor's protocol ID
FinnATOPY
Acronym
FinnATOPY
Status last verified
Oct 2026
First submitted
12 Mar 2024
Last updated
15 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

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