Early detection of bacterial airway infections in children with primary ciliary dyskinesia and cystic fibrosis by electronic nose

Early detection of bacterial airway infections in children with primary ciliary dyskinesia and cystic fibrosis by electronic nose - Detection of airway infections in CF and PCD with the electronic nose

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON33077

Enrollment

170

Registered

2009-08-25

Start date

2009-03-20

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

Cystic Fibrosis immotile cilia syndrome mucoviscoidosis / Primary ciliary dyskinesia

Interventions

None listed

Eligibility

Age

2 Years to 17 Years

Inclusion criteria

Inclusion criteria: Patients: children 0 - 17 years old with cystic fibrosis or primary ciliary dykinesia Healthy controls: children 0 - 17 years old without pulmonary, metabolic, or inflammatory diseases

Exclusion criteria

Exclusion criteria: Patients: metabolic, or inflammatory disorders Healthy controls: pulmonary, metabolic or inflammatory disease

Design outcomes

Primary

Measure	Time frame
The primary outome of this study will be: - the discrimination between CF and PCD patients with and without pulmonary infections - the discrimination between CF, PCD and healthy controls	—

Secondary

Measure	Time frame
none	—

Countries

Netherlands

Outcome results