The electronic nose in the discrimination of parent reported and doctor confirmed wheeze
- Conditions
- asthma1000170810024967
- Registration Number
- NL-OMON31929
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 105
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
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
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary outcome of the study will be:<br /><br>- the discrimination between the various clinically defined subgroups of<br /><br>patients in a so-called *training-set.*<br /><br>- the identification of newly recruited subjects from the same subgroups in a<br /><br>so-called *validation-set*.</p><br>
- Secondary Outcome Measures
Name Time Method <p>not-applicable</p><br>