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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03129399
Other study ID # suny
Secondary ID
Status Recruiting
Phase N/A
First received April 14, 2017
Last updated May 20, 2017
Start date May 20, 2017
Est. completion date June 20, 2018

Study information

Verified date May 2017
Source Shanghai 9th People's Hospital
Contact Yu Sun, MD,PhD
Phone 0086-136-1189-5542
Email dr_sunyu@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was designed to determine the comparison between the King Vision video laryngoscope and McGrath MAC video laryngoscope for nasotracheal intubation.Patients were divided into 2 groups of 40 patients each.Patients of King Vision group [n=40]and Macintosh group [n=40]were intubated using respective devices.This study is the first to search the use of King Vision video laryngoscope for nasotracheal intubation in difficult airway.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date June 20, 2018
Est. primary completion date May 20, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- ASA physical status 1-2

- Scheduled for general anesthesia with nasotracheal intubation

- Cormach-Lehane score 3-4

Exclusion Criteria:

- contraindications to nasal intubation

- Patients with a history of anti-hypertensive drugs

Study Design


Related Conditions & MeSH terms


Intervention

Device:
King Vision video laryngoscope
nasal intubation using King Vision video laryngoscope Device after general anesthesia induction
McGrath MAC video laryngoscope
nasal intubation with McGrath MAC video laryngoscope Device after general anesthesia induction

Locations

Country Name City State
China Shanghai Ninth People's Hospital,Affililated to Shanghai Jiaotong University School of Medicine Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai 9th People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary time to intubation from taking of the intubation device to successful intubation 0 min after nasal intubation
Secondary Hemodynamic changes heart rate 1 min before general anesthesia induction
Secondary Hemodynamic changes heart rate 1 min after general anesthesia induction
Secondary Hemodynamic changes heart rate 3 min after general anesthesia induction
Secondary Hemodynamic changes heart rate 5 min after general anesthesia induction
Secondary ease of intubation VAS scores 5 min after nasal intubation
Secondary incidence of trauma sore throat, hoarseness, etc 24hour after surgery
Secondary incidence of trauma sore throat, hoarseness, etc 1hour after surgery
Secondary number of failures intubation failure 5 min after nasal intubation
Secondary the degree of Cormach-Lehane glottic exposure 5 min after nasal intubation
See also
  Status Clinical Trial Phase
Completed NCT00400972 - Comparison of GlideScope Videolaryngoscopy to Direct Laryngoscopy for Nasal Intubation N/A
Completed NCT02109211 - Does Altering Magill Forceps Affect Nasal Intubation Time N/A
Terminated NCT03032263 - Video vs. Direct Laryngoscopy in Pediatric Nasal Intubation N/A
Recruiting NCT04038762 - Inflation-deflation Method for Nasal Intubation in Pediatric Patients N/A
Completed NCT03126344 - Nasal Intubation Using King Vision Video Laryngoscopy N/A