NCT02411422

Brief Summary

The investigators will compare conventional intubation using Macintosh laryngoscope, blind endotracheal intubation using i-gel for conduit and bronchoscopic intubation using Ambu-aScope and i-gel. All situation assumed as cardiac arrest. i.e, someone give chest compressions continuously without interruption. Moreover the investigators will compare the type of endotracheal tube. Reinforced tube has more soft tube tip, so the investigators think it is more acceptable for intubation using i-gel as conduit.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
23

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2015

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

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 18, 2015

Completed
14 days until next milestone

Study Start

First participant enrolled

April 1, 2015

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2015

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 8, 2015

Completed
Last Updated

April 14, 2015

Status Verified

April 1, 2015

Enrollment Period

Same day

First QC Date

March 18, 2015

Last Update Submit

April 13, 2015

Conditions

Keywords

intubationcardiopulmonary resuscitationmanikins

Outcome Measures

Primary Outcomes (1)

  • intubation time

    1st intubation attempt, an expected average time is 1 min.

    1 Day

Secondary Outcomes (1)

  • success rate for intubation

    1 Day

Study Arms (3)

Intubation using laryngoscope

EXPERIMENTAL

Intubation using Macintosh laryngoscope. we will check procedure time according to kind of endotracheal tube, separately. Two kinds of endotracheal tube will be used * Conventional endotracheal tube * Reinforced endotracheal tube

Device: Conventional endotracheal tubeDevice: Reinforced endotracheal tube

i-gel blind intubation

EXPERIMENTAL

i-gel blind intubation means that blind endotracheal intubation will be performed after i-gel insertion. i-gel will be used as a conduit. we will check procedure time according to kind of endotracheal tube, separately. Two kinds of endotracheal tube will be used * Conventional endotracheal tube * Reinforced endotracheal tube

Device: Conventional endotracheal tubeDevice: Reinforced endotracheal tube

i-gel bronchoscopic intubation

EXPERIMENTAL

i-gel bronchoscopic intubation means that bronchoscopic endotracheal intubation will be performed after i-gel insertion. i-gel will be used as a conduit. we will check procedure time according to kind of endotracheal tube, separately. Two kinds of endotracheal tube will be used * Conventional endotracheal tube * Reinforced endotracheal tube

Device: Conventional endotracheal tubeDevice: Reinforced endotracheal tube

Interventions

Conventional endotracheal tube

Intubation using laryngoscopei-gel blind intubationi-gel bronchoscopic intubation

Reinforced endotracheal tube

Intubation using laryngoscopei-gel blind intubationi-gel bronchoscopic intubation

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • emergency physician
  • work at emergency department more than 1 year.
  • or more experience of endotracheal intubation

You may not qualify if:

  • having backache or wrist pain

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kangnam Sacred Heart Hospital

Seoul, Yeongdeungpo-gu, 150-037, South Korea

Location

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
emergency medicine fellowship

Study Record Dates

First Submitted

March 18, 2015

First Posted

April 8, 2015

Study Start

April 1, 2015

Primary Completion

April 1, 2015

Study Completion

April 1, 2015

Last Updated

April 14, 2015

Record last verified: 2015-04

Locations