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NCT02411422 Clinical Trial

Comparison of Efficiency Between I-gel Blind Intubation and I-gel Bronchoscopic Intubation During Resuscitation

Heart Arrest Clinical Trial

— i-gel_br  

Official title:
Comparison of Efficiency Between I-gel-Assisted Blind Intubation and I-gel-assisted Bronchoscopic Intubation During Cardiopulmonary Resuscitation: Randomized Simulation Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02411422
Other study ID # 2015-02-30
Secondary ID
Status Completed
Phase N/A
First received March 18, 2015
Last updated April 13, 2015
Start date April 2015
Est. completion date April 2015

Study information
Verified date April 2015
Source Hallym University Kangnam Sacred Heart Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 23
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- emergency physician

- work at emergency department more than 1 year.

- 50 or more experience of endotracheal intubation

Exclusion Criteria:

- having backache or wrist pain

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Intervention

Device:
• Conventional endotracheal tube
Conventional endotracheal tube
• Reinforced endotracheal tube
Reinforced endotracheal tube

Locations
Country Name City State
Korea, Republic of Kangnam Sacred Heart Hospital Seoul Yeongdeungpo-gu

Sponsors (1)
Lead Sponsor Collaborator
Hallym University Kangnam Sacred Heart Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary intubation time 1st intubation attempt, an expected average time is 1 min. 1 Day No
Secondary success rate for intubation the rate for successful 1st intubation 1 Day No
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