NCT01312155

Brief Summary

The study investigates assisted intubation using a videolaryngoscope in anesthesia.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2011

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2011

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

March 8, 2011

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 10, 2011

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2012

Completed
Last Updated

October 25, 2013

Status Verified

October 1, 2013

Enrollment Period

11 months

First QC Date

March 8, 2011

Last Update Submit

October 24, 2013

Conditions

Intubation Conditions

Keywords

endotrachealintubationvideotime

Outcome Measures

Primary Outcomes (1)

  • Performance

    Success rate in % of intubation: Number of patients where 'assisted intubation' was successful

    3 months

Secondary Outcomes (1)

  • Time

    3 months

Study Arms (1)

Patients undergoing general anesthesia

Other: Intubation

Interventions

IntubationOTHER

Intubation, endotracheal

Patients undergoing general anesthesia

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients undergoing general anesthesia with endotracheal intubation

You may qualify if:

  • Easy airway assessment

You may not qualify if:

  • Difficult airway
  • ASA 3

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

MUHC

Montreal, Quebec, H3G1A4, Canada

Location

MeSH Terms

Interventions

Intubation

Intervention Hierarchy (Ancestors)

TherapeuticsInvestigative Techniques

Study Officials

  • Thomas Hemmerling, MD

    MUHC - McGill

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

March 8, 2011

First Posted

March 10, 2011

Study Start

March 1, 2011

Primary Completion

February 1, 2012

Study Completion

February 1, 2012

Last Updated

October 25, 2013

Record last verified: 2013-10

Locations

CA(1)