A Peri-intubation Oral Intervention to Reduce Oral Flora and VAP
NCT ID: NCT00248300
Last Updated: 2015-11-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
156 participants
INTERVENTIONAL
2005-08-31
2008-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
TREATMENT
NONE
Interventions
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Chlorhexidine
Chlorhexidine, 5 ml swab to the oral cavity within 12 hours of endotracheal tube intubation
Eligibility Criteria
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Inclusion Criteria
* endotracheal intubation within the past 12 hours
* mechanical ventilation
Exclusion Criteria
* previous endotracheal tube placement in the last 48 hours
* burn injuries
18 Years
ALL
No
Sponsors
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United States Department of Defense
FED
Uniformed Services University of the Health Sciences
FED
TriService Nursing Research Program
OTHER
Virginia Commonwealth University
OTHER
Responsible Party
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Principal Investigators
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Mary Jo E Grap, PhD
Role: PRINCIPAL_INVESTIGATOR
Virginia Commonwealth University School of Nursing
Locations
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Virginia Commonwealth University School of Nursing
Richmond, Virginia, United States
Countries
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References
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Grap MJ, Munro CL, Elswick RK Jr, Sessler CN, Ward KR. Duration of action of a single, early oral application of chlorhexidine on oral microbial flora in mechanically ventilated patients: a pilot study. Heart Lung. 2004 Mar-Apr;33(2):83-91. doi: 10.1016/j.hrtlng.2003.12.004.
Other Identifiers
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MDA-905-03-1-TS02, N03-006
Identifier Type: -
Identifier Source: secondary_id
SToPP-IT
Identifier Type: -
Identifier Source: org_study_id
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