World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT01265862
Date of registration: 21/12/2010
Prospective Registration: Yes
Primary sponsor: Centre hospitalier de l'Université de Montréal (CHUM)
Public title: Does the Use of the GlideRite® Endotracheal Tube in Combination With the I-gel® Improve Intubation Success Rate?
Scientific title: Comparison of LMA-Fastrach® and I-gel® for Tracheal Intubation: Does the Use of the GlideRite® Endotracheal Tube in Combination With the I-gel® Improve Success Rate?
Date of first enrolment: April 2011
Target sample size: 120
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT01265862
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment  
Phase:  N/A
Countries of recruitment
Canada
Contacts
Name:     Nathalie Massicotte, MD, FRCPC
Address: 
Telephone:
Email:
Affiliation:  Centre hospitalier de l'Université de Montréal (CHUM)
Key inclusion & exclusion criteria

Inclusion Criteria:

- Age 18 and older

- Patients undergoing elective surgery under general anesthesia, requiring endotracheal
intubation

Exclusion Criteria:

- American Society of Anesthesiologists (ASA) classification = 4

- Contraindications to muscle relaxation

- Mouth opening less than 2 cm

- Patients at increased risk of regurgitation



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Intubation
General Anesthesia
Intervention(s)
Procedure: Tracheal intubation through I-gel®
Procedure: Tracheal intubation through LMA-Fastrach®
Primary Outcome(s)
First attempt success rate of tracheal intubation [Time Frame: After successful insertion of tracheal tube before the beginning of surgery]
Secondary Outcome(s)
Time needed for successful insertion of a supraglottic device [Time Frame: After insertion of the device before the beginning of surgery]
Time needed to obtain successful tracheal intubation [Time Frame: After tracheal intubation before the beginning of surgery]
First attempt success rate of supraglottic device insertion [Time Frame: After insertion of the device before the beginning of surgery]
Fibreoptic view following the supraglottic device insertion [Time Frame: After insertion of the device before surgery]
Global success rate of supraglottic device insertion [Time Frame: After insertion of the device before the beginning of surgery]
Secondary ID(s)
NM2011-001
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history