Aspiration of Subglottic Secretions Using Hi-Lo Evac Endotracheal Tube: Tube Size and Incidence of Suction Lumen Dysfunction
NCT ID: NCT00450476
Last Updated: 2007-03-22
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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UNKNOWN
60 participants
OBSERVATIONAL
2007-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
Interventions
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Hi-Lo Evac Endotracheal Tube
Eligibility Criteria
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Inclusion Criteria
18 Years
90 Years
ALL
No
Sponsors
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University Hospital, Alexandroupolis
OTHER
Principal Investigators
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Christos K Dragoumanis, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Intensive Care Unit, University Hospital of Alexandroupolis
Locations
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University General Hospital of Alexandroupolis
Alexandroupoli, Evros, Greece
Countries
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Central Contacts
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Other Identifiers
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30/3/25-01-2007
Identifier Type: -
Identifier Source: org_study_id
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