Ultrasonography in Confirming Proper Position of Endotracheal Tube
1 other identifier
observational
80
1 country
1
Brief Summary
The purpose of this study is to assess the applicability of using ultrasonography in confirmation of the position of the endotracheal tube (ETT) after intubated to patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2010
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2010
CompletedFirst Submitted
Initial submission to the registry
June 9, 2011
CompletedFirst Posted
Study publicly available on registry
June 15, 2011
CompletedJune 15, 2011
June 1, 2011
3 months
June 9, 2011
June 14, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The confirmation of ETT depth
A transcricothyroid membrane view of the ultrasonography was chosen for confirmation of ETT depth measurement. Firstly, measured the distance from probe (skin) to anterior surface of ETT. Then, measured the distance from probe (skin) to balloon cuff level. Finally the depth of ETT (Distance from vocal cord to balloon cuff) was calculated by using Pythagorus rule.
1 hour
Secondary Outcomes (1)
The confirming the presence of ETT in airway.
1 hour
Study Arms (1)
Intubate
Interventions
Eligibility Criteria
The patients who visited the emergency department, Siriraj hospital and needed ETT intubation as their adequate treatment. In the period from September 2010 to November 2010.
You may qualify if:
- age \>18 years old with either endotracheal or nasotracheal intubation
- having normal airway anatomy
- performed portable CXR after intubation
You may not qualify if:
- presence in history of neck radiation, cervical spine immobility/instability
- unstable vital signs
- unwilling to participate or denial of informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Anesthesiology Department
Bangkok, 10700, Thailand
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Phuriphong Songarj, MD
Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
June 9, 2011
First Posted
June 15, 2011
Study Start
September 1, 2010
Primary Completion
December 1, 2010
Study Completion
December 1, 2010
Last Updated
June 15, 2011
Record last verified: 2011-06