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NCT01209559 Clinical Trial

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

Airway Management Clinical Trial

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT01209559
Other study ID # CDHA-RS/2011-156
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 2011
Est. completion date January 2011

Study information
Verified date July 2018
Source Nova Scotia Health Authority
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 2011
Est. primary completion date January 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Canada QEII Health Sciences Centre Halifax Nova Scotia

Sponsors (1)
Lead Sponsor Collaborator
Nova Scotia Health Authority

Country where clinical trial is conducted

Canada, 

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