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Gender and Proper Size of Oropharyngeal Airway: Pilot Study

Not Applicable
Completed
Conditions
Adult Patients Undergoing Surgery That Requires General Anesthesia
Interventions
Device: No. 7 oral airway
Device: No. 8 oral airway
Device: No. 9 oral airway
Registration Number
NCT02326753
Lead Sponsor
Yonsei University
Brief Summary

The purpose of this study is to assess the adequacy of mask ventilation with the different sized-oropharyngeal airway.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria
  • adult patients undergoing surgery that requires general anesthesia
Exclusion Criteria
  • anticipated difficult intubation
  • patients without teeth or with loose teeth
  • cervical spine disease
  • body mass index over 35 kg/m2
  • pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
No. 7 oral airwayNo. 7 oral airway-
No. 8 oral airwayNo. 8 oral airway-
No. 9 oral airwayNo. 9 oral airway-
Primary Outcome Measures
NameTimeMethod
the proportion of patients whose oropharyngeal airway is properup to 10 minutes after the start of anesthetic induction

The oropharyngeal airway will be inserted into the patient's mouth. Investigators will check the laryngeal view using fiberoptic bronchoscope and the adequacy of ventilation after the investigator ventilates the patient using the face mask. If both the laryngeal view and ventilation are appropriate, the size of oropharyngeal airway will be considered as the proper size for the patient.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department of Anesthesiology and Pain MedicineSeverance Hospital, Yonsei University Health System

🇰🇷

Seoul, Korea, Korea, Republic of

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