eus(bijholten)problemen bij kinderen met Cystic Fibrosis.
- Conditions
- Cystic Fibrosis (CF)
- Registration Number
- NL-OMON23697
- Lead Sponsor
- Haga Teaching Hospital
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Confirmed diagnosis of Cystic Fibrosis based on genotyping or a positive sweat test
- Age 0-<18 years
Exclusion Criteria
- Gross inmmunodeficiency (congenital or acquired)
- Congenital mucociliary problems other than CF (e.g. Primary Ciliairy Diskinesia)
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Opacification of sinuses on CT-scan (Lund-Mackay score)
- Secondary Outcome Measures
Name Time Method - Development of paranasasl sinuses <br /><br>- Severity of CF<br /><br>- Onset of sinonasa pathology<br /><br>- Symptoms of sinonasal disease<br /><br>- Outcome of nasopharyngeal swab<br /><br>- Anatomic variations in sinonasal area<br /><br>- Outcome of lower airway culture<br />