Aspiration of Subglottic Secretions Using Hi-Lo Evac Endotracheal Tube: Tube Size and Incidence of Suction Lumen Dysfunction
1 other identifier
observational
60
1 country
1
Brief Summary
To evaluate the correlation between endotracheal tube size and incidence of dysfunction of suction lumen of Hi-Lo Evac endotracheal tube in critically ill patients who required mechanical ventilation for more than 48 hours.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2007
CompletedFirst Submitted
Initial submission to the registry
March 21, 2007
CompletedFirst Posted
Study publicly available on registry
March 22, 2007
CompletedMarch 22, 2007
March 1, 2007
March 21, 2007
March 21, 2007
Conditions
Keywords
Interventions
Eligibility Criteria
You may qualify if:
- Critically ill patients with orotracheal intubation and anticipated duration of intubation more than 48 hours
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University General Hospital of Alexandroupolis
Alexandroupoli, Evros, 68100, Greece
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Christos K Dragoumanis, MD, PhD
Intensive Care Unit, University Hospital of Alexandroupolis
Central Study Contacts
Study Design
- Study Type
- observational
- Time Perspective
- OTHER
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
March 21, 2007
First Posted
March 22, 2007
Study Start
January 1, 2007
Last Updated
March 22, 2007
Record last verified: 2007-03