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The electronic nose in the discrimination of parent reported and doctor confirmed wheeze

The electronic nose in the discrimination of parent reported and doctor confirmed wheeze - The electronic nose in the assesment of wheeze

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31929
Enrollment
105
Registered
2008-08-21
Start date
2008-08-01
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

asthma

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

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

MeasureTime 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

MeasureTime frame
not-applicable

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)