asthma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients: Informed consent obtained from parents age between 0 and 2 years;Healthy controls: Informed consent obtained from parents age between 0 and 2 years
Exclusion criteria
Exclusion criteria: Patients: Present metabolic or syndrom disorder Underlying respiratory tract disease, like congenital airway abnormalities, cystic fibrosis, primary ciliary dyskinesia, bronchopulmonary dysplasia or bronchiectasis;Healthy controls: Present metabolic or syndrome disorder Respiratory tract disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the study will be: - the discrimination between the various clinically defined subgroups of patients in a so-called *training-set.* - the identification of newly recruited subjects from the same subgroups in a so-called *validation-set*. | — |
Secondary
| Measure | Time frame |
|---|---|
| not-applicable | — |
Countries
Netherlands