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Trial registered on ANZCTR
Registration number
ACTRN12611000038998
Ethics application status
Approved
Date submitted
10/01/2011
Date registered
12/01/2011
Date last updated
12/01/2011
Type of registration
Prospectively registered
Titles & IDs
Public title
Effect of endotracheal tube on ventilator associated pneumonia in Intensive Care Unit patients
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Scientific title
Effect of EVAC endotracheal tube on decreasing ventilator associated pneumonia in critically ill patients admitted to Intensive Care Units
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Secondary ID [1]
253371
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Trial has not a secondary ID.
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Universal Trial Number (UTN)
U1111-1118-9359
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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
260909
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Condition category
Condition code
Infection
259047
259047
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0
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Other infectious diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intubation of patients with EVAC oral endotracheal tube.(A specific tube with a distal lumen for suctioning of subglottic secretions and very thin cuff with poly urethane material which has not any folds on it after cuff filling). Patients will be intubated minimum 3 days until they will meet extubation criteria.
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Intervention code [1]
257809
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Prevention
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Comparator / control treatment
Intubation of patients with standard oral endotracheal tubes(Polyvinyl Chloride portex tubes with high volum and low pressure cuff),and will be intubated minimum 3 days until they will meet extubation criteria.
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Control group
Active
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Outcomes
Primary outcome [1]
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Ventilator Associated Pneumonia will be assessed by CIPS(Clinically infectione Pulmonary Score).If the score is more than 6 the patient has VAP.
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Assessment method [1]
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Timepoint [1]
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During Intensive Care Unit(ICU) stay
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Secondary outcome [1]
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Mortality
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Assessment method [1]
268784
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Timepoint [1]
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During Intensive Care Unit Stay
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Eligibility
Key inclusion criteria
Adult patients(more than 18 years old) who will be ventilated for more than 3 days
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Minimum age
18
Years
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Maximum age
80
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
previous history of mechanical ventilation,pregnancy, Human Immunodefficiency Virus infection, malignancy,Immunosuppressive therapy, leukocyte count less than 1000/mm3
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Study design
Purpose of the study
Prevention
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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)
Sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Permuted block randomisation
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Masking / blinding
Open (masking not 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
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/02/2011
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Actual
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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
90
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Iran, Islamic Republic Of
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State/province [1]
3133
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Tabriz University of Medical Sciences
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Address [1]
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Golgasht street, Tabriz
5157663114
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Country [1]
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Iran, Islamic Republic Of
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Primary sponsor type
University
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Name
Tabriz University of Medical Sciences
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Address
Golgasht street, Tabriz
5157663114
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Country
Iran, Islamic Republic Of
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Secondary sponsor category [1]
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None
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Name [1]
257469
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Address [1]
257469
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Country [1]
257469
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Ethics committee of Tabriz Medical University
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Ethics committee address [1]
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University of Tabriz,Daneshgah street, Tabriz 515766114
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Ethics committee country [1]
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Iran, Islamic Republic Of
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Date submitted for ethics approval [1]
260273
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Approval date [1]
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11/12/2010
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Ethics approval number [1]
260273
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5/04/7376
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Summary
Brief summary
Almost 10-28% of patients admitted to intensive Care Units(ICU) suffered from Ventilator Associated Pneumonia(VAP) which leads to increasing mortality,ICU length of stay and mortality. As micro or macroaspiration of subglottic secretions is one of the most important risk factors for developing VAP, adevice that can suction these secretion may help to decreasing VAP. So in this study we want to evaluate the efficacy of EVAC endotracheal tube in decreasing VAP in critical ill patients. ninty patients will be enrolled in this study. patient will be allocated to two 45 patient groups. One group will be intubated with EVAC endotracheal tube and the other group will be intubated with standard tube. the Vap rate, mortality, ICU length of stay and duration of mechanical ventilation will be noted for each patient.
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Trial website
there is not any website for trial
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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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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 public queries
Name
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ata mahmoodpoor
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Address
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General ICU, Shohada hospital,El-Goli ave, Tabriz
5157663114
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Country
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Iran, Islamic Republic Of
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Phone
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00989141160888
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Ata Mahmoodpoor
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Address
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General ICU, Shohada hospital,El-Goli ave, Tabriz
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Country
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Iran, Islamic Republic Of
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Phone
6241
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00989141160888
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Fax
6241
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Email
6241
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[email protected]
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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
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
A prospective randomized trial of tapered-cuff endotracheal tubes with intermittent subglottic suctioning in preventing ventilator-associated pneumonia in critically ill patients.
2017
https://dx.doi.org/10.1016/j.jcrc.2016.11.007
N.B. These documents automatically identified may not have been verified by the study sponsor.
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