Comparison of Conventional Lightwand Intubation Versus Video-laryngoscope Guided Lightwand Intubation in Simulated Cervical Spine-immobilized Patients
NCT ID: NCT03169556
Last Updated: 2017-10-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
318 participants
INTERVENTIONAL
2016-12-19
2017-10-13
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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video-laryngoscope guided lightwand
Video-laryngoscope guided lightwand
After anesthetic induction,the difficult airway is simulated by wearing a semi-hard neck collar. For intubation, video-laryngoscope is inserted into the oral cavity ntil the epiglottis tip was visible without lifting the epiglottic vallecula. Then, the endotracheal tube with lightwand is inserted toward the midline under the epiglottis and the intubation is performed looking the transilluminated light of lightwand.
lightwand
lightwand alone
After anesthetic induction,the difficult airway is simulated by wearing a semi-hard neck collar. Then, the endotracheal tube with lightwand is inserted and the intubation is performed with conventional method (blind technique by confirming transillumination).
Interventions
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Video-laryngoscope guided lightwand
After anesthetic induction,the difficult airway is simulated by wearing a semi-hard neck collar. For intubation, video-laryngoscope is inserted into the oral cavity ntil the epiglottis tip was visible without lifting the epiglottic vallecula. Then, the endotracheal tube with lightwand is inserted toward the midline under the epiglottis and the intubation is performed looking the transilluminated light of lightwand.
lightwand alone
After anesthetic induction,the difficult airway is simulated by wearing a semi-hard neck collar. Then, the endotracheal tube with lightwand is inserted and the intubation is performed with conventional method (blind technique by confirming transillumination).
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Patients scheduled surgery under the general anesthesia
Exclusion Criteria
2. Patients with body mass index \>35kg/m2, hemodynamic instability or loosening teeth
3. Patient who disagrees to participate this study or lacks decision-making ability, illiteracy, or foreigner
4. American Society of Anesthesiologists physical status ≥ 3
20 Years
80 Years
ALL
Yes
Sponsors
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Yonsei University
OTHER
Responsible Party
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Locations
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Department of Anesthesiology and Pain Medicine, Severance Hospital, Yonsei University College of Medicine
Seoul, , South Korea
Countries
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Other Identifiers
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1-2016-0069
Identifier Type: -
Identifier Source: org_study_id