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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02224027
Other study ID # apsj0821
Secondary ID
Status Recruiting
Phase N/A
First received August 21, 2014
Last updated December 28, 2015
Start date August 2014
Est. completion date December 2016

Study information

Verified date December 2015
Source Yeungnam University College of Medicine
Contact Sangjin Park, M.D.
Phone 82-53-620-3366
Email apsj0718@naver.com
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The use of laryngeal mask airway or i-gel to manage airway may improve success rates, especially in difficult situations more than tracheal intubation.


Description:

This study compares the insertion success rate and insertion time among the proceal laryngeal mask airway, i-gel, and tracheal tube. Following a short lecture, airway novices try to insert proceal laryngeal mask airway, i-gel, and tracheal tube into manikin with difficult laryngoscopy scenarios.


Recruitment information / eligibility

Status Recruiting
Enrollment 109
Est. completion date December 2016
Est. primary completion date October 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- medical student

- nurse

- no experience of insertion using tracheal tube, i-gel, and laryngeal mask airway

Exclusion Criteria:

- experience of insertion using tracheal tube, i-gel, and laryngeal mask airway

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Device:
proceal laryngeal mask airway
In proceal laryngeal mask group, proceal laryngeal mask airway is inserted by novices.
tracheal tube
In tracheal tube group, tracheal tube is intubated by novices.
i-gel
In i-gel group, i-gel is inserted by novices.

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Yeungnam University hospital Daegu

Sponsors (1)

Lead Sponsor Collaborator
Yeungnam University College of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary the time of successful laryngeal mask, i-gel, or tracheal tube insertion attempt A blinded observer records the time of successful laryngeal mask, i-gel, or tracheal tube insertion attempt. intraoperative No
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