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A Comparative Study of the Air-Q ILA and the ILMA for Ventilation and Intubation

This study has suspended participant recruitment.
(Study never initiated.)
Sponsor:
Information provided by (Responsible Party):
Orlando Hung, Capital District Health Authority, Canada
ClinicalTrials.gov Identifier:
NCT01209559
First received: September 23, 2010
Last updated: October 31, 2011
Last verified: October 2011

September 23, 2010
October 31, 2011
January 2011
December 2011   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT01209559 on ClinicalTrials.gov Archive Site
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A Comparative Study of the Air-Q ILA and the ILMA for Ventilation and Intubation
Not Provided

The objective of this study is to determine if the glottic view obtained with the air-Q Intubating Laryngeal Airway (air-Q ILA, Cookgas LLC®, Mercury Medical®, Clearwater, FL, USA) is better than that obtained with the traditionally used intubating laryngeal mask airway (LMA FastrachTM or ILMA, LMA North America Inc., San Diego, CA). The study will also compare effectiveness of ventilation.

Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
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Probability Sample

Healthy ASA class I and II patients scheduled for elective surgery under general anesthesia requiring the use of the LMA.

Airway Management
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  • air-Q Intubating Laryngeal Airway
  • LMA FastrachTM or ILMA
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Suspended
60
December 2011
December 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • healthy ASA class I and II patients scheduled for elective surgery under general anesthesia requiring the use of the LMA

Exclusion Criteria:

  • history of acid reflux,
  • a BMI ≥ 40kg.m-2,
  • require endotracheal intubation,
  • have predictors of difficult intubation,
  • not candidates for insertion of an ILMA or LMA, including a mouth opening of less than 2.5 cm,
  • cannot consent to the study
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT01209559
CDHA-RS/2011-156
Not Provided
Orlando Hung, Capital District Health Authority, Canada
Capital District Health Authority, Canada
Not Provided
Not Provided
Capital District Health Authority, Canada
October 2011

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