Assessment of the clinical impact of related (clonal) Pseudomonas aeruginosa strains in people with cystic fibrosis (CF).
- Conditions
- Clonal P. aeruginosa infection in patients with cystic fibrosis.Infection - Studies of infection and infectious agentsHuman Genetics and Inherited Disorders - Cystic fibrosis
- Registration Number
- ACTRN12607000349448
- Lead Sponsor
- A/Prof Scott Bell (Principle Investigator)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 1500
Children, adolescents and adults (both males and females) with CF who can produce a spontaneously expectorated sputum sample with evidence of P. aeruginosa (this will apply to both the Prevalence and Observational Studies). 2) Following the Cross sectional Study, only those patients without evidence of clonal strains will continue to have samples and clinical data collected for the Observational Study.
1) Patient's that are unable to produce a spontaneously expectorated sputum sample or those who have no evidence of P. aeruginosa. 2) Patient's with evidence of a clonal strain at the completion of the Prevalence Study, will not be included in the Observational Study. 3) Any patient that is unable or unwilling to provide written informed consent.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method