Gender and Proper Size of Oropharyngeal Airway: Pilot Study
- Conditions
- Adult Patients Undergoing Surgery That Requires General Anesthesia
- Interventions
- Device: No. 7 oral airwayDevice: No. 8 oral airwayDevice: 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
- adult patients undergoing surgery that requires general anesthesia
- 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
Group Intervention Description No. 7 oral airway No. 7 oral airway - No. 8 oral airway No. 8 oral airway - No. 9 oral airway No. 9 oral airway -
- Primary Outcome Measures
Name Time Method the proportion of patients whose oropharyngeal airway is proper up 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
Name Time Method
Trial Locations
- Locations (1)
Department of Anesthesiology and Pain MedicineSeverance Hospital, Yonsei University Health System
🇰🇷Seoul, Korea, Korea, Republic of