We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Airway Management and Vascular Access Simulation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00892671
First Posted: May 4, 2009
Last Update Posted: August 30, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of Alabama at Birmingham
  Purpose
This project involves a pre- and post- airway management and vascular access simulation survey. The purpose of the study is to assess the perceived effectiveness of the simulation course on the performance of medical students enrolling in the Anesthesiology rotation during their third and fourth year of medical education.

Condition Intervention
Airway Management Vascular Access Other: Simulation

Study Type: Observational
Official Title: Airway Management and Vascular Access Simulation

Further study details as provided by University of Alabama at Birmingham:

Primary Outcome Measures:
  • perceived effectiveness [ Time Frame: pre- and post- simulation ]

Estimated Enrollment: 50
Study Start Date: October 2008
Study Completion Date: October 2009
Primary Completion Date: October 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
medical students Other: Simulation
simulation of airway management and vascular access

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
third and fourth year medical studens enrolling in the UAB Department of Anesthesiology rotation
Criteria

Inclusion Criteria:

  • medical student enrolled in the Department of Anesthesiology rotation

Exclusion Criteria:

  • anyone not enrolled in the rotation
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00892671


Locations
United States, Alabama
University of Alabama at Birmingham
Birmingham, Alabama, United States, 35249
Sponsors and Collaborators
University of Alabama at Birmingham
Investigators
Principal Investigator: Thomas R. Vetter, MD, MPH University of Alabama at Birmingham Department of Anesthesiology
  More Information

Responsible Party: Thomas R. Vetter, PI, UAB Department of Anesthesiology
ClinicalTrials.gov Identifier: NCT00892671     History of Changes
Other Study ID Numbers: E080829003
First Submitted: April 30, 2009
First Posted: May 4, 2009
Last Update Posted: August 30, 2010
Last Verified: August 2010

Keywords provided by University of Alabama at Birmingham:
Perceived effectiveness