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.
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.
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
- Conditions
- Asthma, Asthma in Children, Allergy, Rhinitis, Allergic, Atopic Dermatitis, Allergen Immunotherapy
- 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 group | Role | What they receive |
|---|---|---|
| Atopic | Patientes with any atopic condition (g.e., asthma, atopic dermatitis, IgE-mediateid allergy) Receives: Other: No intervention; Other: No Intervention: Observational Cohort | |
| Control group - migrane | Patients with migrane Receives: Other: No intervention; Other: No Intervention: Observational Cohort | |
| Control group - celiac disease | Patients with celiac disease Receives: Other: No intervention; Other: No Intervention: Observational Cohort | |
| Control group - UTI | Patients with urinary tract infection Receives: Other: No intervention; Other: No Intervention: Observational Cohort | |
| Control group - LRTI | Patients with lower respiratory tract infection Receives: Other: No intervention; Other: No Intervention: Observational Cohort | |
| Control group - bronchitis | Patients 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.
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
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
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
Use and effectiveness of allergen immunotherapy in real world setting
Real world evidence data using specific cohorts
Measured: 7 years
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.
- First posted26 Mar 2024
- Study start1 Dec 2026 (estimated)
- Primary completionDec 2032 (estimated)
- Study completionDec 2034 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AsthmaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
Sponsor and investigators
- Lead sponsor
- Tampere University
- Sponsor type
- University, hospital or other
- Collaborators
- Professor Lauri Lehtimäki, Professor Mika Mäkelä, Professor Sanna Toppila-Salmi, Professor Ilkka Junttila
- Responsible party
- Principal investigator, Peter Csonka, Tampere University
- Investigators
- Péter Csonka, Principal investigator, Tampere University
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