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Laryngoscope Asssited Lightwand Intubation

Not Applicable
Conditions
Cervical Spine Surgery
Interventions
Procedure: Laryngoscope assisted lightwand intubation
Procedure: Lightwand intubation
Registration Number
NCT01950702
Lead Sponsor
Seoul National University Hospital
Brief Summary

To evaluate the success rate for intubation of laryngocope assisted lightwand intubation.

Detailed Description

Light wand intubation is well known for safety intubation in cervical injury patiets. Traditional method of using light wand can damage the supraglottic cavity by scooping the apparatus. The investigators try to evaluate the efficacy of laryngoscope assisted light wand intubation compared to traditional method of using light wand alone.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
168
Inclusion Criteria
  • Patient scheduled for cervical spine surgery under general anesthesia
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Exclusion Criteria
  • congenital or acquired abnormalities of the upper airway, tumours, polyps, trauma, abscesses, inflammation, or foreign bodies in the upper airway
  • history of gastro-esophageal reflux disease, previous airway surgery, an increased risk of aspiration, coagulation disorders
  • American Society of Anesthesiologists physical status ≥ 3
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Laryngoscope assisted lightwand intubationLaryngoscope assisted lightwand intubationAfter standard total intravenous anesthesia using propofol and remifentanil continuous infusion, lightwand intubation using specific device(Macintosh laryngosope, female:3/Male:4) was done by pre-specified anesthesiologist who experienced more than 100 times of laryngoscope assisted lightwand intubation.
Lightwand intubationLightwand intubationAfter standard total intravenous anesthesia using propofol and remifentanil continuous infusion, traditional lightwand intubation was done by pre-specified anesthesiologist who experienced more than 100 times of lightwand intubation. Patient's head were fixed at neutral position during all intubation period.
Primary Outcome Measures
NameTimeMethod
The success rate of intubationup to 60 seconds

confirm the success intubation via end tidal CO2 measurement

Secondary Outcome Measures
NameTimeMethod
The times of scooping of lightwandwithin 1min after insertion of lightwand

Within 1min after insertion of lightwand into oral cavity, check the scooping time of lightwand during intubation.

lightwand search (=intubation) timefrom the insertion of the lightwand or laryngoscope into the oral cavity to the point of transillumination over the cricothyroid membrane within 60 sec.

Check the time(sec) from insertion of the lightwand or laryngoscopy into the oral cavity to push the endotracheal tube into the trachea.

Trial Locations

Locations (1)

Seoul National University of Hospital

🇰🇷

Seoul, Jongno-Gu, Korea, Republic of

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