Conventional antimicrobial susceptibility testing
OtherSubjects in this arm will be prescribed 14 days of an intravenous 2 drug antibiotic combination based on conventional planktonic antimicrobial susceptibility testing results.
NCT Number: NCT00786513
The purpose of this study is to determine whether choosing antibiotics based on a biofilm antimicrobial susceptibility assay rather than a conventional planktonic antimicrobial susceptibility assay to treat CF patients with chronic P. aeruginosa infection with an acute pulmonary exacerbation is a safe intervention that will result in improved microbiological and clinical outcomes and decrease markers of pulmonary inflammation.
Looking for future studies?
Notify MeAll sexes
Interventional
Phase 2
BC Children's Hospital, Vancouver, British Columbia, Canada
Cystic fibrosis (CF) is the most common fatal genetic condition in the Caucasian population and affects over 3,000 Canadians. Respiratory failure caused by chronic pulmonary infection is the primary cause of death in CF patients. The improved life expectancy of CF patients in the past several decades is due in part to the more aggressive use of antibiotics in the treatment of respiratory infections. However, there is currently no antimicrobial susceptibility assay that can predict which antibiotics will result in improved patient outcomes. Since Pseudomonas aeruginosa is known to grow as a resistant biofilm in the CF lung, antimicrobial susceptibility testing based on biofilm growth of P. aeruginosa may lead to different antibiotic choices that significantly decrease the pulmonary bacterial density of P. aeruginosa. A biofilm antimicrobial susceptibility assay thus has the ability to change the way antibiotics are chosen to treat CF patients and result in improved lung function and longer lives for all CF patients.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subjects in this arm will be prescribed 14 days of an intravenous 2 drug antibiotic combination based on conventional planktonic antimicrobial susceptibility testing results.
Subjects in this arm will be prescribed 14 days of an intravenous 2 drug antibiotic combination based on biofilm antimicrobial susceptibility testing results.
Time frame: Measured at day 0 and day 14 of antibiotic treatment and at the 1 month follow-up visit
Time frame: Measured at day 0, day 7, and day 14 of antibiotic treatment and at the 1 month follow-up visit
Time frame: 1 year following the completion of antibiotic therapy
Time frame: Measued at day 0 and day 14 of antibiotic treatment and at the 1 month follow-up visit
Time frame: Meaured at day 0 and day 14 of antibiotic treatment and at the 1 month follow-up visit
The Hospital for Sick Children
Other
Randomized Double Blind Controlled Trial of the Use of a Biofilm Antimicrobial Susceptibility Assay to Guide Antibiotic Therapy in Chronic Pseudomonas Aeruginosa Infected Cystic Fibrosis Patients
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.
Published trials that share one or more normalized conditions with this study.
NCT05453578
Bacterial Disease Carrier, Bacterial Infections
Tucson, Arizona, United States
View Trial DetailsNCT04970225
Bacterial Infections, Bacterial Infections and Mycoses
Paris, France
View Trial DetailsNCT00700050
Bacterial Infections, Bacterial Infections and Mycoses
Toronto, Ontario, Canada
View Trial DetailsNCT02295566
Bacterial Infections, Bacterial Infections and Mycoses
Southampton, Hampshire, United Kingdom
View Trial Details