None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients scheduled for elective surgery under general anesthesia Patients with a body mass index greater than 30 kg/m2 Patients classified as American Society of Anesthesiology Physical Classification (ASA PS) 2 or 3 Patients between the ages of 20 and 80 Patients who have voluntarily provided written consent to participate in the clinical trial
Exclusion criteria
Exclusion criteria: Patients scheduled for oral and nasal surgery Patients with a history or expectation of difficult airway intubation and airway ventilation, other than obesity Patients who need to restrict cervical movement due to an unstable cervical spine Patients with a history of head and neck surgery Patients with a mouth opening of less than 2.5 cm Patients at high risk of aspiration pneumonia (with symptomatic or untreated gastroesophageal reflux disorder and hiatal hernia) Pregnant patients Other patients deemed unsuitable for the trial by the researcher
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time taken to insert the supraglottic airway | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of attempts at insertion of the supraglottic airway;Ease of insertion of the supraglottic airway;Confirmation of the appropriate placement of the supraglottic airway | — |
Countries
Korea, Republic of
Contacts
Chonnam National University Hospital