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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03215823
Other study ID # 1-2017-0035
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 17, 2017
Est. completion date November 14, 2018

Study information

Verified date February 2019
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The usefulness of videolaryngoscope has been verified by several studies, and the frequency of videolaryngoscopy is increasing in clinical practice. Data on the use of videolaryngoscopes, however, were not sufficiently accumulated when compared with data on the use of previously used macintosh laryngoscopes. In addition, videolaryngoscopy increases the success rate of endotracheal intubation compared to conventional macintosh laryngoscopy, but endotracheal intubation with videolaryngoscope is not successful in all cases with one intubation attempt. Therefore, if the difficult endotracheal intubation with the videolaryngoscope can be predicted in advance, it may be possible to improve the success rate of intubation by reducing unnecessary use of the videolaryngoscope and preparing other equipment. There are many studies on the preoperative examination that can predict the difficulty of intubation when using a macintosh laryngoscope. However, there are still attempts to find screening tests that predict precisely the difficult endotracheal intubation because the accuracy of screening tests is not high. In particular, there is a lack of research on factors that can predict difficult endotracheal intubation when using videolaryngoscope. Therefore, the investigators aimed to investigate the factors predictive of difficult endotracheal intubation when attempting intubation using videolaryngoscope.


Recruitment information / eligibility

Status Completed
Enrollment 808
Est. completion date November 14, 2018
Est. primary completion date November 14, 2018
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria:

1. Patients who are scheduled for endotracheal intubation using a videolaryngoscope for general anesthesia

Exclusion Criteria:

1. Patients who are planned to receive awake intubation

2. Patients who have a tracheostomy tube

3. Patients who do not cooperate in evaluating the head and neck due to mental retardation

4. Trauma patient wearing a neck collar due to cervical fracture

5. Pregnancy

Study Design


Related Conditions & MeSH terms

  • Endotracheal Intubation Using Videolaryngoscope for General Anesthesia

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (3)

Han DW, Shim YH, Shin CS, Lee YW, Lee JS, Ahn SW. Estimation of the length of the nares-vocal cord. Anesth Analg. 2005 May;100(5):1533-5, table of contents. — View Citation

Reed DB, Clinton JE. Proper depth of placement of nasotracheal tubes in adults prior to radiographic confirmation. Acad Emerg Med. 1997 Dec;4(12):1111-4. — View Citation

Stoneham MD. The nasopharyngeal airway. Assessment of position by fibreoptic laryngoscopy. Anaesthesia. 1993 Jul;48(7):575-80. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary the occurrence of the difficult endotracheal intubation when using a videolaryngoscope. logistic regression analysis will be used to find out the predictors of the difficult endotracheal intubation. 10 minutes during the induction of general anesthesia.