Prevalence of Chronic Rhinosinusitis in Cystic Fibrosis

NCT ID: NCT00266474

Last Updated: 2014-12-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

187 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-12-31

Study Completion Date

2007-09-30

Brief Summary

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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.

Detailed Description

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Conditions

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Cystic Fibrosis Sinusitis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Cross sectional CF study

Multicentric study, including 187 CF patients of all age groupr in 5 CF centres.

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

Intervention Type OTHER

Interventions

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

Intervention Type OTHER

Other Intervention Names

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nasal lavage and induced sputum

Eligibility Criteria

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Inclusion Criteria

* Subject has a confirmed diagnosis of cystic fibrosis

Exclusion Criteria

* current systemic therapy against Pseudomonas aeruginosa
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Jena

OTHER

Sponsor Role lead

Responsible Party

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PD Dr. Jochen G. Mainz

Head of CF Center, Pediatric Pulmonology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jochen G. Mainz, M.D.

Role: STUDY_CHAIR

University of Jena

Locations

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Friedrich-Schiller-Universität

Jena, Thuringia, Germany

Site Status

Countries

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Germany

References

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Mainz JG, Naehrlich L, Schien M, Kading M, Schiller I, Mayr S, Schneider G, Wiedemann B, Wiehlmann L, Cramer N, Pfister W, Kahl BC, Beck JF, Tummler B. Concordant genotype of upper and lower airways P aeruginosa and S aureus isolates in cystic fibrosis. Thorax. 2009 Jun;64(6):535-40. doi: 10.1136/thx.2008.104711. Epub 2009 Mar 11.

Reference Type BACKGROUND
PMID: 19282318 (View on PubMed)

Other Identifiers

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CF_Sinusitis_QS

Identifier Type: -

Identifier Source: org_study_id