None listed
Conditions
Interventions
Medical Device : The principal investigator will assign each study participant to either the control group or the experimental group based on a random allocation table. The random allocation table wil
Sponsors
The Catholic University of Korea, Eunpyeong St. Mary's Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Female patients aged =20 years and <75 years
Exclusion criteria
Exclusion criteria: Patients in whom anatomical difficulty is anticipated for insertion of either an endotracheal tube or a supraglottic airway device (i-gel), such as congenital or acquired malformations of the oral cavity or pharynx, or loose teeth. Patients with severe obesity, defined as a body mass index (BMI) = 35 kg/m². Patients with a history of severe gastroesophageal reflux disease (GERD). Patients with impaired pulmonary function and chronic lung disease resulting in markedly reduced lung compliance. Patients with a history of complications related to supraglottic airway device placement or endotracheal intubation during previous surgeries or anesthesia. Patients who do not consent to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Leak Fraction | — |
Secondary
| Measure | Time frame |
|---|---|
| Oropharyngeal leak pressure;Intraoperative airway and respiratory complications between the two groups | — |
Countries
Korea, Republic of
Contacts
Public ContactJi Young Min
The Catholic University of Korea
Outcome results
None listed