7-Year asthma study aims to uncover hidden disease patterns
NCT ID NCT06163807
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 1,200 adults with asthma (with or without nasal polyps) for up to 7 years to see how their condition changes over time. Researchers will track symptoms, treatments, and biomarkers in blood and breath. The goal is to better understand different types of asthma and improve future care.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 1,200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with asthma (intermittent, mild, moderate or severe asthma according to the GINA classification), with or without nasal polyposis attended third-level hospitals of the Spanish National Health System.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: For the general asthma cohort (MEGA): * Age from 18 to 80 y.o. with asthma with and without nasal polyposis based on GINA guidelines (compatible clinical symptoms+reversibility of at least 12% and 200 mL in FEV1 after the administration of 200-400 μg albuterol/salbutamol or positive methacholine test) of several severities attended at participant centres * Already in follow-up in MEGA cohort * To participate in the study * Signed informed consent Inclusion criteria for asthma patients treated with biologics * Patients from 18 to 80 y.o. with uncontrolled asthma with and without nasal polyposis that fulfil criteria to be treated with biological drugs (Existing treatment with medium-to-high-dose ICS (≥ 250 μg of fluticasone propionate twice daily or equipotent ICS daily dosage to a maximum of 2000 μg/day of fluticasone propionate or equivalent) in combination with a second controller (e.g., LABA, LTRA) for at least 3 months+ airflow limitation- FEV1 \<80%/FEV1/FVC \<70+ACQ-5 score ≥ 1.5/ ACT \< 19 at inclusion and/or have experience any of the following events on the last year: treatment with systemic steroids/ hospitalization or emergency medical care visit for worsening asthma. * When planning dupilumab, mepolizumab, benralizumab or reslizumab, biomarker levels, and exacerbation in the previous year will be considered according to the Spanish Ministry of Health recommendations for reimbursement of any biological drug in severe asthma. In the case of Omalizumab allergic asthma and IgE \> 75 and \< 1500 UI * Patients already in follow-up in the cohort of patients treated with biologics * Willing to participate in the study * Sign informed consent Exclusion Criteria: * Exclusion criteria for MEGA COHORT * Diagnosis of chronic obstructive pulmonary disease or other lung disease that may impair lung function * Comorbid disease that might interfere with the evaluation, e.g. psychiatric disorders * Patients participating in other clinical trials * Patients without the capacity to understand the aim of the study * Exclusion criteria for asthma patients treated with biologics * Diagnosis of chronic obstructive pulmonary disease or other lung disease that may impair lung function * Comorbid disease that might interfere with the evaluation, e.g. psychiatric disorders * Patients participating in other clinical trials * Patients without the capacity to understand the aim of the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
8 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Clinic
RECRUITINGBarcelona, BARCELONA, 08036, Spain
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Hospital Del Ferrol
RECRUITINGA Coruña, LA CORUÑA, 15405, Spain
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Hospital Universitari Vall de Hebron
RECRUITINGBarcelona, BARCELONA, 08035, Spain
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Hospital Universitario Germans Trias
RECRUITINGBadalona, BARCELONA, 08916, Spain
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Hospital Universitario La Paz
RECRUITINGMadrid, Madrid, 28046, Spain
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Hospital Universitario Sant Pau
RECRUITINGBarcelona, BARCELONA, 08041, Spain
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Hospital Universitario Santiago de Compostela
RECRUITINGSantiago de Compostela, Acoruña, 15706, Spain
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Hospital Universitario de Navarra
RECRUITINGPamplona, Navarre, 31008, Spain
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