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OpenTrials
Completed

NCT Number: NCT00266474

Prevalence of Chronic Rhinosinusitis in Cystic Fibrosis

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject has a confirmed diagnosis of cystic fibrosis

Exclusion criteria

  • current systemic therapy against Pseudomonas aeruginosa

Treatment and study plan

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

Other

Other names: nasal lavage and induced sputum

Primary outcomes

  1. Pathogen colonization in upper and lower airways

    Time frame: 3yrs

  2. Sinonasal symptoms (SNOT-20)

    Time frame: 3 yrs

  3. rhinomanometry and rhinoscopy

    Time frame: 3yrs

Sponsors and collaborators

Lead sponsor

University of Jena

Other

Registry information

Important dates

Study start
2005
Study completion
2007
First posted
Dec 16, 2005
Registry last updated
Dec 4, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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