Comparison Airway Devices in Nasotracheal Intubation in Manikin (MGR-AR2010A1)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Manuel Ángel Gómez-Ríos, Complexo Hospitalario Universitario de A Coruña
ClinicalTrials.gov Identifier:
NCT01311284
First received: March 7, 2011
Last updated: January 3, 2012
Last verified: January 2012

March 7, 2011
January 3, 2012
March 2011
December 2011   (final data collection date for primary outcome measure)
Time in seconds required for a successful intubation attempt with the Macintosh laryngoscope, Airtraq NT and Mcgrath. [ Time Frame: Two months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01311284 on ClinicalTrials.gov Archive Site
  • Time visualization of the glottis [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • Intubation time [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • The duration of the first intubation attempt (whether successful or not) [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • Number of intubation attempts. [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • The success rate of placement of the endotracheal tube (ETT) in the trachea [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • Cormack and Lehane Grade [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • Number of operators needed [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • Severity of dental trauma [ Time Frame: Two months ] [ Designated as safety issue: No ]
  • Satisfaction of the operators [ Time Frame: Two months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Comparison Airway Devices in Nasotracheal Intubation in Manikin
Comparison of Airtraq Nasotracheal Mcgrath and Macintosh Laryngoscope in Nasotracheal Intubation: A Manikin Study

Nasotracheal intubation is usually required in oral surgery to allow an unrestricted surgical approach. The standard method is generally performed using the Macintosh laryngoscope supported by Magill forceps. However, it is recommended to perform awake tracheal intubation in situations where a difficult airway is predicted, a scenario where this technique may be poorly tolerated by the patient. Although fibreoptic intubation is considered the "gold standard", sometimes it is difficult to perform and,therefore, alternatives are necessary. The hypothesis is that optical laryngoscopes as the Airtraq nasotracheal and Mcgrath can improve the time and/or success of nasotracheal intubation in a manikin.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Nasotracheal Intubation
  • Device: Macintosh laryngoscope, Airtraq NT, Mcgrath laryngoscope
    Each participant will use the Macintosh laryngoscope (blade No. 3), laryngoscope Airtraq NT and Mcgrath Laryngoscope under conditions of normal and difficult airway in different simulated scenarios.
    Other Names:
    • Macintosh
    • Airtraq NT
    • Mcgrath
  • Device: Macintosh laryngoscope
    intubate with the macintosh laryngoscope
  • Device: McGrath
    Intubate with McGrath device
  • Device: Airtraq Nasotracheal
    intubate with Airtraq Nasotracheal
  • Active Comparator: Macintosh
    Interventions:
    • Device: Macintosh laryngoscope, Airtraq NT, Mcgrath laryngoscope
    • Device: Macintosh laryngoscope
  • Active Comparator: Mcgrath
    Interventions:
    • Device: Macintosh laryngoscope, Airtraq NT, Mcgrath laryngoscope
    • Device: McGrath
  • Active Comparator: Airtraq Nasotracheal
    Interventions:
    • Device: Macintosh laryngoscope, Airtraq NT, Mcgrath laryngoscope
    • Device: Airtraq Nasotracheal

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
63
December 2011
December 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Be Component of service of anesthesiology C.H.U. A Coruña
  • Give voluntary consent to participate in the study

Exclusion Criteria:

  • Not meet the above criteria
Both
23 Years to 65 Years
No
Contact information is only displayed when the study is recruiting subjects
Spain
 
NCT01311284
MGR-AR-2010-A1
No
Manuel Ángel Gómez-Ríos, Complexo Hospitalario Universitario de A Coruña
Manuel Ángel Gómez-Ríos
Not Provided
Not Provided
Complexo Hospitalario Universitario de A Coruña
January 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP