Tracheal IntubationNCT02074098
Endotracheal Intubation Using Macintosh Laryngoscope, Glidescope, Airwayscope During Chest Compression With Adjustment Height of a Bed
A study testing Macintosh laryngoscope, Glidescope and Airwayscope in people with Tracheal Intubation and Cardiac Arrest, run by Hanyang University at 1 site in South Korea.
Trial summary
The purpose of this study is to determine whether a bed height make an effect to endotracheal intubation with Macintosh laryngoscope, Glidescope and Airwayscope during chest compressions in- hospital simulation cardiac arrest. Read more about this study
- Who is it for?
- Ages 18 to 60 yearsHealthy volunteers can take part
- Conditions the study is for
- Tracheal Intubation, Cardiac Arrest
- What is being tested?
- Macintosh laryngoscope, Glidescope and Airwayscope
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 21 participants
- Where
- 1 siteSouth Korea
- Study dates
- Mar 2014to Mar 2014
- Phase
- Interventional
- 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 60 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Experience of Intubation > 50 times
- Postgraduates year 1,2,3,4 and Emergency physicians in emergency department
Who cannot join
- Wrist or low back disease
Trial locations and contacts
1 site in 1 country.
About this study
The purpose of this study is to determine whether a bed height make an effect to endotracheal intubation with Macintosh laryngoscope, Glidescope and Airwayscope during chest compressions in- hospital simulation cardiac arrest.
- Conditions
- Tracheal Intubation, Cardiac Arrest
- Being tested
- Macintosh laryngoscope, Glidescope, Airwayscope
- Keywords
- intubation, Cardiopulmonary resuscitation, Manikin study
- Medical subject headings
- Heart Arrest
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Macintosh laryngoscopeDevice
Direct Laryngoscope
GlidescopeDevice
Videolaryngoscope-1
AirwayscopeDevice
Videolaryngoscope-2
| Study group | Role | What they receive |
|---|---|---|
| a 65 cm bed height | Experimental | 1) Bed height : approximately 65cm (Lowest) Receives: Device: Macintosh laryngoscope; Device: Glidescope; Device: Airwayscope |
| a 95cm bed height | Experimental | 2) Bed height : approximately 95cm (highest) Receives: Device: Macintosh laryngoscope; Device: Glidescope; Device: Airwayscope |
What is being measured
The primary outcome is the main question the study is designed to answer.
To measure a time to expose the glottis view with a laryngoscope
Measured: 1 day
To measure a time to intubate the tube with a laryngoscope
Measured: 1 day
To estimate the success rate of Intubation
" Failure " means that tube is inserted in esophagus and the time is over than 120 seconds
Measured: 1 day
Secondary outcomes (1)
To assess the grade for the glottis view with a laryngoscopy
Using the Cormack-Lehane Grade system
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Feb 2014 (estimated)
- Study startMar 2014
- Primary completionMar 2014
- Study completionMar 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Tracheal IntubationStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 21 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hanyang University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jaehoon Oh, Hanyang University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02074098
- Sponsor's protocol ID
- Intubation with a bed height
- Status last verified
- Mar 2014
- First submitted
- 20 Feb 2014
- Last updated
- 18 Mar 2014
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 18 Mar 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Endotracheal Intubation Using Macintosh Laryngoscope, Glidescope, Airwayscope During Chest Compression With Adjustment Height of a Bed
- ClinicalTrials.gov ID
- NCT02074098
- Acronym / sponsor ID
- Intubation with a bed height
- Conditions
- Tracheal Intubation, Cardiac Arrest
- Keywords
- intubation, Cardiopulmonary resuscitation, Manikin study
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 21 participants (actual)
- Lead sponsor
- Hanyang UniversityUniversity, hospital or other
- Study start
- Mar 2014
- Primary completion
- Mar 2014 (actual)
- Study completion
- Mar 2014 (actual)
- First posted
- 28 Feb 2014 (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 purpose of this study is to determine whether a bed height make an effect to endotracheal intubation with Macintosh laryngoscope, Glidescope and Airwayscope during chest compressions in- hospital simulation cardiac arrest.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| a 65 cm bed height | Experimental | Device: Macintosh laryngoscope, Device: Glidescope, Device: Airwayscope1) Bed height : approximately 65cm (Lowest) |
| a 95cm bed height | Experimental | Device: Macintosh laryngoscope, Device: Glidescope, Device: Airwayscope2) Bed height : approximately 95cm (highest) |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- Experience of Intubation > 50 times
- Postgraduates year 1,2,3,4 and Emergency physicians in emergency department
Key exclusion criteria (1 listed)
- Wrist or low back disease
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 |
|---|---|---|
| Macintosh laryngoscopeDirect Laryngoscope | Device | a 65 cm bed height, a 95cm bed height |
| GlidescopeVideolaryngoscope-1 | Device | a 65 cm bed height, a 95cm bed height |
| AirwayscopeVideolaryngoscope-2 | Device | a 65 cm bed height, a 95cm bed height |
Primary outcome
To measure a time to expose the glottis view with a laryngoscope
Time frame: 1 day
To measure a time to intubate the tube with a laryngoscope
Time frame: 1 day
To estimate the success rate of Intubation
Time frame: 1 day
" Failure " means that tube is inserted in esophagus and the time is over than 120 seconds
1 secondary outcome
To assess the grade for the glottis view with a laryngoscopy
Time frame: 1 day
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 18 Mar 2014.
Related trials for Tracheal Intubation
Not yet recruitingObservational study
AI-assisted Tracheal Intubation in Children
Intubation
Not yet recruiting
AI Smart Glasses Feedback for Intubation Training in Medical Students
Intubation, Intratracheal, Medical Education
Recruiting
Development and Preliminary Validation of Intelligent Video Laryngoscope for Emergency Use
Critically Ill Patients Requiring Mechanical Ventilation
Recruiting
Hyperangulated vs. Macintosh Style Blades for Intubation in Obstetric Patients
Obstetric, Cesarean Birth
Recruiting
Smart Checklist Implementation for Pediatric Tracheal Intubations in the ICU- Multicenter Study
Intubation Complication
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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Macintosh laryngoscope, Glidescope and Airwayscope in people with Tracheal Intubation and Cardiac Arrest, run by Hanyang University at 1 site in South Korea.
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 2 inclusion and 1 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 18 Mar 2014. 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 South Korea. 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?
To measure a time to expose the glottis view with a laryngoscope (time frame: 1 day). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 18 Mar 2014.