Prevalence of Chronic Rhinosinusitis in Cystic Fibrosis

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00266474

Enrollment

187

Registered

2005-12-16

Start date

2005-12-31

Completion date

2007-09-30

Last updated

2014-12-04

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

Conditions

Cystic Fibrosis, Sinusitis

Keywords

Cystic Fibrosis with Chronic Rhinosinusitis

Brief summary

Aim of the study is to detect the prevalence of chronic rhinosinusitis and the colonisation with Pseudomonas aerug. in the upper airways in patients with cystic fibrosis.

Interventions

OTHERAssessment of upper and lower airway colonization, sinonasal symptoms, history, rhinoscopy and rhinomanometry.

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* Subject has a confirmed diagnosis of cystic fibrosis

Exclusion criteria

* current systemic therapy against Pseudomonas aeruginosa

Design outcomes

Primary

Measure	Time frame
Pathogen colonization in upper and lower airways	3yrs
Sinonasal symptoms (SNOT-20)	3 yrs
rhinomanometry and rhinoscopy	3yrs

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026