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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON26592

Enrollment

120

Registered

2011-04-11

Start date

2011-05-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Primary ciliary dyskinesia Cystic fibrosis

Interventions

No intervention, cross sectional study.

Eligibility

Inclusion criteria

Inclusion criteria: Patients: Children 0-17 years with cystic fibrosis or primary ciliary dyskinesia. 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
1. Discrimination of CF-/PCD-patients with and without pulmonary infections; 2. Discrimination of CF-/PCD-patients from healthy controls.	—

Secondary

Measure	Time frame
Discrimination of different classes (aerobic, anaerobic, gram positive, gram negative strains), or types of bacteria responsible for the infection in vivo.	—

Contacts

Public ContactT. Paff

Postbus 7057

t.paff@vumc.nl+31 (0)20 4445491

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)