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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00447109
Registration number
NCT00447109
Ethics application status
Date submitted
12/03/2007
Date registered
14/03/2007
Date last updated
14/03/2007
Titles & IDs
Public title
Time Interval for Changing Closed System Suction Catheters, Effect on Ventilator Associated Pneumonia
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Scientific title
Endotracheal Suction With or Without Daily Changes of Closed System Suction. Effect on Ventilator Associated Pneumonia and Cost
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Secondary ID [1]
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T10308
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Secondary ID [2]
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122/02
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pneumonia, Ventilator Associated
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Closed System Suction Catheter
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Condition category
Condition code
Respiratory
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Other respiratory disorders / diseases
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Infection
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Other infectious diseases
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Infection
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Studies of infection and infectious agents
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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ventilator-associated pneumonia
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [1]
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length of hospital
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [2]
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intensive care stay
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Assessment method [2]
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Timepoint [2]
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Secondary outcome [3]
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duration of mechanical ventilation
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Assessment method [3]
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Timepoint [3]
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Secondary outcome [4]
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hospital mortality
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Assessment method [4]
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Timepoint [4]
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Secondary outcome [5]
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number of acquired organ system derangements
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Assessment method [5]
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Timepoint [5]
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Secondary outcome [6]
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cost of the closed system suction catheters
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Assessment method [6]
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Timepoint [6]
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Eligibility
Key inclusion criteria
* Aged greater than 18 years
* Mechanically ventilated for more than 24 hours
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
* Admitted from other hospital already mechanically ventilated
* Massive haemoptysis
* Previously received mechanical ventilation
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
NA
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/09/2003
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
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The Alfred Hospital - Melbourne
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Recruitment postcode(s) [1]
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3181 - Melbourne
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Funding & Sponsors
Primary sponsor type
Government body
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Name
Bayside Health
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Address
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Country
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Other collaborator category [1]
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Other
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Name [1]
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Deakin University
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of this study was to compare the incidence of ventilator-associated pneumonia between two groups of patients randomised to have closed system suction catheter changes every 24 hours and patients having closed system suction catheter changes every seven days or as required.
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Trial website
https://clinicaltrials.gov/study/NCT00447109
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Lauren J McTier
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Address
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Deakin University
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00447109
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