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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00803881
Other study ID # CF_Sinusitis_LS
Secondary ID
Status Recruiting
Phase N/A
First received December 5, 2008
Last updated October 24, 2016
Start date December 2008
Est. completion date December 2018

Study information

Verified date October 2016
Source University of Jena
Contact Jochen Mainz, MD
Phone +49 3641 938425
Email Jochen.Mainz@med.uni-jena.de
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial Summary

Aim of the study is to detect the prevalence of chronic rhinosinusitis, pathogen colonization of the lower and upper airways and, in a sub-cohort the sense of smelling in patients with cystic fibrosis.


Description:

The sub-study on the sense of smelling in CF has been finalized in the meantime. Results were published in 2012:

Smell in cystic fibrosis. Lindig J, Steger C, Beiersdorf N, Michl R, Beck JF, Hummel T, Mainz JG. Eur Arch Otorhinolaryngol. 2013 Mar;270(3):915-21. doi: 10.1007/s00405-012-2124-2. Epub 2012 Aug 14.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date December 2018
Est. primary completion date July 2018
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Subject has a confirmed diagnosis of cystic fibrosis

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
nasal lavage and sputum collection
non-invasive longitudinal assessment of pathogen colonization in both airway levels

Locations

Country Name City State
Germany University of Jena - CF-Center Jena

Sponsors (1)

Lead Sponsor Collaborator
University of Jena

Country where clinical trial is conducted

Germany, 

References & Publications (4)

Lindig J, Steger C, Beiersdorf N, Michl R, Beck JF, Hummel T, Mainz JG. Smell in cystic fibrosis. Eur Arch Otorhinolaryngol. 2013 Mar;270(3):915-21. doi: 10.1007/s00405-012-2124-2. Epub 2012 Aug 14. — View Citation

Mainz JG, Hentschel J, Schien C, Cramer N, Pfister W, Beck JF, Tümmler B. Sinonasal persistence of Pseudomonas aeruginosa after lung transplantation. J Cyst Fibros. 2012 Mar;11(2):158-61. doi: 10.1016/j.jcf.2011.10.009. Epub 2011 Nov 30. — View Citation

Mainz JG, Michl R, Pfister W, Beck JF. Cystic fibrosis upper airways primary colonization with Pseudomonas aeruginosa: eradicated by sinonasal antibiotic inhalation. Am J Respir Crit Care Med. 2011 Nov 1;184(9):1089-90. — View Citation

Mainz JG, Naehrlich L, Schien M, Käding M, Schiller I, Mayr S, Schneider G, Wiedemann B, Wiehlmann L, Cramer N, Pfister W, Kahl BC, Beck JF, Tümmler 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. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Dynamics in CF upper and lower airway colonization with pathogens longitudinal non-invasive sampling of upper and lower airways in CF 10 years No
Primary Assessment of ability to smell in CF patients 3 years No
Secondary pulmonary function / BMI 10 years No
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