King Vision and Cervical Spines Movement

NCT01914601 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 29

Last updated 2016-08-09

No results posted yet for this study

Summary

Extensive cervical spines movement during endotracheal intubation can result in serious neurological injury, especially in the patients with unrecognized cervical spines injury.\[1-2\] Moreover, direct laryngoscopy may be difficult if spine movement is limited because of arthritis, disc disease or a small gap between the occiput and the spinous process of the atlas.\[3-4\]

Video laryngoscopes allow for intubation without alignment of the oral, pharyngeal, and tracheal axes which minimize the cervical movements, especially in the patients with restricted cervical movements. \[5,6\] Compared with the Macintosh laryngoscope, the use of AirWay Scope decreases median upper cervical-spine movement during intubation under in-line stabilization in patients with normal cervical-spine. \[6\] Unfortunately, the use video laryngoscopes are associated with longer times to tracheal intubation compared with the traditional techniques which may be attributed to the variable learning curves of the practitioners. \[7-9\]

The King Vision video laryngoscope® (King Systems Company, a division of Consort Medical, Indianapolis, Indiana, USA) is an anatomically shaped, rigid laryngoscope that uses fiberoptic technology to view the larynx with micro camera offers a 160 degree of view potentially eliminating the need for neck flexion and head extension. \[10\]

To the best of the authors' knowledge, there is no study has evaluated the King vision laryngoscope regarding the neck movement during routine tracheal intubation under general anesthesia.

Conditions

  • Need Tracheal Intubation

Interventions

DEVICE

Macintosh-King Vision

laryngoscopy will be performed with the Macintosh followed by the King Vision laryngoscope

DEVICE

King Vision-Macintosh

laryngoscopy will be performed with the King Vision followed by the Macintosh laryngoscope.

Sponsors & Collaborators

  • Mansoura University

    collaborator OTHER
  • Imam Abdulrahman Bin Faisal University

    lead OTHER

Principal Investigators

  • Abdulmohsen Al Ghamdi, MD · Associate Professor/Chairman of Anesthesiology

  • Mohamed R El Tahan, MD · Associate Professor of Anesthesiology

  • Alaa M Khidr, MD · Assistant Professor of Anesthesiology

  • Abdullah s Al Mulhim, MD · Demonstrator of Radiology

  • Samah A El Kenany, MD · Lecturer of Anesthesiology, Mansoura University, Egypt

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2015-12-31
Completion
2016-01-31

Countries

  • Egypt
  • Saudi Arabia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01914601 on ClinicalTrials.gov