Ultrasonography in Confirming Proper Position of Endotracheal Tube

Sponsor
Mahidol University (Other)
Overall Status
Completed
CT.gov ID
NCT01373437
Collaborator
(none)
80
1
3
26.8

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Ultrasonography (Sonosite )

Detailed Description

To assess the applicability of using ultrasonography as compared to routine portable CXR in confirmation of ETT position.

To determine the accuracy of ultrasonography in measuring the depth of ETT as compare to standard CXR method.

Study Design

Study Type:
Observational
Actual Enrollment :
80 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Ultrasonography in Confirming Proper Position of Endotracheal Tube in Emergency Department at Siriraj Hospital: Applicability and Accuracy
Study Start Date :
Sep 1, 2010
Actual Primary Completion Date :
Dec 1, 2010
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Intubate

Device: Ultrasonography (Sonosite )
Sonosite MICROMAXXTM with linear probe L38e/10-5 MHz

Outcome Measures

Primary Outcome Measures

  1. The confirmation of ETT depth [1 hour]

    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.

Secondary Outcome Measures

  1. The confirming the presence of ETT in airway. [1 hour]

    A transcricothyroid membrane view was chosen for confirmation of ETT position. Various glottic structures such as True Vocal Cord (TVC), False Vocal Cord (FVC), and arythenoid cartilage can be visualized.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age >18 years old with either endotracheal or nasotracheal intubation

  • having normal airway anatomy

  • performed portable CXR after intubation

Exclusion Criteria:
  • presence in history of neck radiation, cervical spine immobility/instability

  • unstable vital signs

  • unwilling to participate or denial of informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Anesthesiology Department Bangkok Thailand 10700

Sponsors and Collaborators

  • Mahidol University

Investigators

  • Study Director: Phuriphong Songarj, MD, Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01373437
Other Study ID Numbers:
  • 345/2553(EC4)
First Posted:
Jun 15, 2011
Last Update Posted:
Jun 15, 2011
Last Verified:
Jun 1, 2011

Study Results

No Results Posted as of Jun 15, 2011