Laryngeal Mask Airway With Video-stylet

Anesthesia; Functional Clinical Trial

Official title:

Video Stylet Guided Laryngeal Mask Airway Insertion in Pediatrics: a Randomized Controlled Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT02937337
• Other study ID #: H-1609-090-792
• Status: Not yet recruiting
• Phase: N/A
• First received: October 17, 2016
• Last updated: October 18, 2016
• Start date: October 2016
• Est. completion date: October 2017

Study information

• Verified date: October 2016
• Source: Seoul National University Hospital
• Contact: Hee-Soo Kim, professor
• Phone: 02-2072-3664
• Is FDA regulated: No
• Health authority: South Korea: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

In this randomized controlled trial, we aimed to compare the efficacy of video-stylet guided laryngeal mask airway real time insertion technique with the standard recommended index finger-guided insertion technique in pediatric patients.

Description:

Compare the efficacy and safety of using video-stylet guided laryngeal mask airway insertion with blind technique

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 108
• Est. completion date: October 2017
• Est. primary completion date: October 2017
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 2 Years to 6 Years

Eligibility

Inclusion Criteria:

• pediatric patients undergoing general anesthesia using laryngeal mask airways

Exclusion Criteria:

• recent (within 2 weeks) upper respiratory infection

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Anesthesia; Functional

Intervention

Device:
• Laryngeal mask insertion with videostylet guided technique

• Laryngeal mask insertion with standard blind technique

Locations

Country	Name	City	State
Korea, Republic of	SNUH	Seoul	Jongro Gu

Sponsors (1)

Lead Sponsor	Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	the time required for inserting the laryngeal mask airways		time interval between the caregiver picked up and put down the laryngeal mask airway an expected average of 30 seconds	No
Secondary	the numbers of insertion attempt		interval between the caregiver picked up and put down the laryngeal mask airway an expected average of 30 seconds	No