Utility of Bedside Ultrasound in the Prediction of Difficult Airway
This study has been completed.
Sponsor:
University of Nebraska
Collaborator:
The Association for Medical Ultrasound
Information provided by:
University of Nebraska
ClinicalTrials.gov Identifier:
NCT00799357
First received: November 26, 2008
Last updated: January 11, 2010
Last verified: January 2010
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Purpose
A variety of pre-intubation clinical screening tests have been advocated to predict difficult laryngoscopy, but their usefulness is limited in emergency department, intensive care unit, pre-hospital and combat settings. Patients in these settings are often confused, lethargic, obtunded, uncooperative and common screening tests for difficult laryngoscopy cannot be applied in a large number of emergency intubations. In the recent past, there has been growing interest in upper airway ultrasound. The purpose of this study is to assess the utility of bedside ultrasound to predict difficult airway in patients requiring emergency intubation.
| Condition |
|---|
|
Laryngoscopy |
| Study Type: | Observational |
| Study Design: | Time Perspective: Cross-Sectional |
| Official Title: | Utility of Bedside Ultrasound in the Prediction of Difficult Airway |
Further study details as provided by University of Nebraska:
Primary Outcome Measures:
- Predictors of difficult laryngoscopy [ Time Frame: one day ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 162 |
| Study Start Date: | December 2008 |
| Study Completion Date: | June 2009 |
| Primary Completion Date: | June 2009 (Final data collection date for primary outcome measure) |
Eligibility| Ages Eligible for Study: | 19 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
Pre-op patients
Criteria
Inclusion Criteria:
- Patients scheduled for any surgery under general anesthesia with endotracheal intubation
Exclusion Criteria:
- Upper airway pathologies (facial fractures, tumours, etc)
- Cervical spine fractures
- Tracheostomy tube
- unable to give consent
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00799357
Locations
| United States, Nebraska | |
| University of Nebraska Medical Center | |
| Omaha, Nebraska, United States, 68198 | |
Sponsors and Collaborators
University of Nebraska
The Association for Medical Ultrasound
Investigators
| Principal Investigator: | Srikar R Adhikari | University of Nebraska |
More Information
Publications:
| Responsible Party: | Srikar Adhikari, University of Nebraska Medical Center |
| ClinicalTrials.gov Identifier: | NCT00799357 History of Changes |
| Other Study ID Numbers: | 526-08-EP |
| Study First Received: | November 26, 2008 |
| Last Updated: | January 11, 2010 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Nebraska:
|
ultrasound |
ClinicalTrials.gov processed this record on May 16, 2013