Intubation ConditionsNCT01312155

Assisted Intubation

An observational study of Intubation Conditions, run by McGill University Health Centre/Research Institute of the McGill University Health Centre at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

The study investigates assisted intubation using a videolaryngoscope in anesthesia. Read more about this study

Who is it for?: Ages 18 to 90 years
Conditions the study is for: Intubation Conditions
What is being tested?: Intubation
How many people: 12 participants
Where: 1 siteCanada
Study dates: Mar 2011to Feb 2012
Phase: Observational
Are there results?: None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

Ages 18 to 90 years
All sexes
No healthy volunteers
Adult, Older adult

Study population: Patients undergoing general anesthesia with endotracheal intubation

Who may be able to join

Easy airway assessment

Who cannot join

Difficult airway
ASA 3

Trial locations and contacts

1 site in 1 country.

Canada1 site

MUHC
Montreal, Quebec, H3G1A4

Other trials in Canada

About this study

The study investigates assisted intubation using a videolaryngoscope in anesthesia.

Conditions: Intubation Conditions
Being tested: Intubation
Keywords: endotracheal, intubation, video, time

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

IntubationOther
Intubation, endotracheal

Study groups in NCT01312155
Study group	Role	What they receive
Patients undergoing general anesthesia		Not described Receives: Other: Intubation

What is being measured

The primary outcome is the main question the study is designed to answer.

Performance
Success rate in % of intubation: Number of patients where 'assisted intubation' was successful
Measured: 3 months

Secondary outcomes (1)

Time
Time to intubate: time in sec between insertion of scope into mouth and insertion of endotracheal tube through vocal cords
Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

Mar 2011Feb 2012

First posted10 Mar 2011 (estimated)
Study startMar 2011
Primary completionFeb 2012
Study completionFeb 2012

Resources

Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
Other trials for Intubation ConditionsStudies of the same condition, open and under way.
What the trial phases meanHow a treatment moves from first tests in people to approval.

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design

Study type: Observational
Observational model: Case-control
Time perspective: Prospective
Enrolment: 12 participants (actual)

IDs, dates and publications

ClinicalTrials.gov ID: NCT01312155
Sponsor's protocol ID: 10-338
Status last verified: Oct 2013
First submitted: 8 Mar 2011
Last updated: 25 Oct 2013
Results posted: No
Data monitoring committee: No

Study at a glance

From the registry record, last updated by the sponsor on 25 Oct 2013. Recruitment status is as the sponsor reported it: confirm with the study team.

Official title: Assisted Intubation
ClinicalTrials.gov ID: NCT01312155
Acronym / sponsor ID: 10-338
Conditions: Intubation Conditions
Keywords: endotracheal, intubation, video, time
Study type: Observational
Recruitment status: Completed
Enrolment: 12 participants (actual)
Lead sponsor: McGill University Health Centre/Research Institute of the McGill University Health CentreUniversity, hospital or other
Study start: Mar 2011
Primary completion: Feb 2012 (actual)
Study completion: Feb 2012 (actual)
First posted: 10 Mar 2011 (estimated)
Results: Not posted in the source record

Clinical summary

The research question as the sponsor registered it. This describes what the study plans to test, not what it found.

The study investigates assisted intubation using a videolaryngoscope in anesthesia.

Study design

Observational model: Case-control
Time perspective: Prospective
Number of arms: 1

Arm	Type	Receives
Patients undergoing general anesthesia	–	Other: Intubation

Who may qualify

Ages: 18 to 90 years
Sex: All
Healthy volunteers: Not accepted
Age groups: Adult, Older adult
Study population: Patients undergoing general anesthesia with endotracheal intubation

Key inclusion criteria (1 listed)

Easy airway assessment

Key exclusion criteria (2 listed)

Difficult airway
ASA 3

Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.

Interventions

Intervention	Type	Arms
IntubationIntubation, endotracheal	Other	Patients undergoing general anesthesia

Primary outcome

Performance
Time frame: 3 months
Success rate in % of intubation: Number of patients where 'assisted intubation' was successful

1 secondary outcome

Time
Time frame: 3 months

Results and safety

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

Research links

Official record on ClinicalTrials.govLast updated by the sponsor 25 Oct 2013.

Referral and contact

AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.

Thomas Hemmerling, MD principal investigator

MUHC - McGill

1 site in 1 country: see every site and its status.

Questions about this trial

What is this clinical trial studying?

An observational study of Intubation Conditions, run by McGill University Health Centre/Research Institute of the McGill University Health Centre at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Oct 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Performance (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01312155.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Oct 2013; AzTrials last refreshed its copy on 27 Oct 2026.