TCHCCT-Zhong-Xing-Emergency-Department-airway

Intubation;Difficult Clinical Trial

— TT  

Official title:

TCH-Zhong-Xing-Branch-Emergency-Department

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03366311
• Other study ID #: TCHCCT-ZXER
• Status: Recruiting
• Phase: N/A
• First received: November 27, 2017
• Last updated: December 8, 2017
• Start date: November 27, 2017
• Est. completion date: November 30, 2019

Study information

• Verified date: December 2017
• Source: Taipei City Hospital
• Contact: Tzu-Yao Hung, MD
• Phone: 886-979305599
• Email: bryansolitude[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To investigate which shapes of stylet, hand techniques and possible condition that improve intubation successful rate and reduce the elapsed intubation time.

Description:

Challenging airway is always a big issue in emergency room. However, better hand technique, stylet shapes and conditions affecting intubation successful rate, elapsed duration need further investigations. We compare two endotracheal tube holding position, two holding places, with or without epiglottis lift technique in this study. All intubation processes in the study will be recorded.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 45
• Est. completion date: November 30, 2019
• Est. primary completion date: November 30, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• care givers with sufficient understanding of airway anatomy and management

Exclusion Criteria:

Related Conditions & MeSH terms

• Airway Complication of Anesthesia
• Emergencies
• Intubation;Difficult

Intervention

Procedure:
• holding position
two types of holding positions plus two types of shapes of stylet, with or without epiglottis lift

Locations

Country	Name	City	State
Taiwan	Taipei City Hospital Zhong-Xing branch	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
Taipei City Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	intubation successful rate	intubation more than 90 seconds considered as a failed intubation	through study completion, and average of 15minutes
Secondary	intubation elapsed time	from insertion of endotracheal to the tube until proper placement of endotracheal tube	through study completion, and average of 15minutes
Secondary	insertion elapsed time	from proper glottic view to the tube until proper placement of endotracheal tube	through study completion, and average of 15minutes
Secondary	difficulty of intubation	Visual Analogue Scale with a 10cm bar	through study completion, and average of 15minutes