Comparison of Different Video Laryngoscopes in a Manikin With Immobilized Cervical Spine

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
J. Hinkelbein, University of Cologne
ClinicalTrials.gov Identifier:
NCT01210092
First received: September 27, 2010
Last updated: September 21, 2011
Last verified: September 2011
  Purpose

To determine whether different video laryngoscopes facilitate intubation in an manikin with immobilized cervical spine compared with standard laryngoscopy.


Condition
Tracheal Intubation

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Comparison of Different Video Laryngoscopes in a Manikin With Immobilized Cervical Spine

Resource links provided by NLM:


Further study details as provided by University of Cologne:

Primary Outcome Measures:
  • successful tracheal intubation [ Time Frame: max 5 minutes ] [ Designated as safety issue: No ]

Estimated Enrollment: 25
Study Start Date: August 2010
Study Completion Date: January 2011
Primary Completion Date: November 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts
Macintosh #3 Laryngoscope
Glidescope
Ambu Pentax AWS
McGrath
Airtraq
Storz C-MAC

  Eligibility

Ages Eligible for Study:   25 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

anaesthesiologists

Criteria

Inclusion Criteria:

  • anaesthesiologist
  • experienced in tracheal intubation

Exclusion Criteria:

  • missing experience in tracheal intubation
  • missing informed consent
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01210092

Locations
Germany
Department of Anaesthesiology and Postoperative Critical Care
Cologne, Germany, 50937
Sponsors and Collaborators
University of Cologne
Investigators
Principal Investigator: Wolfgang A Wetsch, MD Department of Anaesthesiology, University of Cologne
  More Information

No publications provided

Responsible Party: J. Hinkelbein, PD Dr. med., University of Cologne
ClinicalTrials.gov Identifier: NCT01210092     History of Changes
Other Study ID Numbers: 10-182-2
Study First Received: September 27, 2010
Last Updated: September 21, 2011
Health Authority: Germany: Local Ethics Board

ClinicalTrials.gov processed this record on September 18, 2014