Prophylaxis of Ventilator Associated Pneumonia by Continuous Lateral Rotation Therapy
NCT ID: NCT00529776
Last Updated: 2008-06-11
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
NA
150 participants
INTERVENTIONAL
2005-09-30
2008-05-31
Brief Summary
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Patients are randomized to CLRT or supine position if mechanically ventilated and not suffering from pneumonia or ARDS within 48 hours after intubation. Prophylaxis of VAP is standardized in both groups. Primary endpoint is incidence of VAP, secondary endpoints are length of ventilation, length of stay and mortality.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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1
Continuous lateral rotation therapy
Continuous lateral rotation therapy
2
Standard manual positioning (Supine position)
No interventions assigned to this group
Interventions
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Continuous lateral rotation therapy
Eligibility Criteria
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Inclusion Criteria
* Intubated not longer than 48 h
* Medical cause for ICU admission
* Expected to be ventilated for \> 48 hours
Exclusion Criteria
* Postoperative patient
18 Years
89 Years
ALL
No
Sponsors
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Medical University of Vienna
OTHER
Responsible Party
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Medical University of Vienna
Principal Investigators
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Thomas Staudinger, MD
Role: PRINCIPAL_INVESTIGATOR
Department of Internal Medicine I, Medical University of Vienna, Austria
Thomas Staudinger, MD
Role: PRINCIPAL_INVESTIGATOR
Dept. of Internal Medicine I, Medical University of Vienna
Locations
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Vienna General Hospital, Medical University of Vienna
Vienna, , Austria
Countries
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Other Identifiers
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EK 38/2004
Identifier Type: -
Identifier Source: org_study_id
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