Comparison of the efficiency of oral airway and nasal airway inserted in the oral airway during mask ventilation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0001756

Enrollment

Registered

2016-01-06

Start date

2016-07-25

Completion date

Unknown

Last updated

2020-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : In both groups, mask ventilation will be performed after intravenous injection of 2 mg/kg propofol. Before mask ventilation, oral airway will be inserted in the oral cavity in group O

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The patients who will undergo elective surgery under general anesthesia in Seoul National University Bundang Hospital. ASA class I or II The patients who agree to participate in this study

Exclusion criteria

Exclusion criteria: American society of Anesthesiologists class over III Risk of difficult mask ventilation The patients who needs awake intubation Risk of regurgitation and pulmonary aspiration Craniofacial anomaly The patients who reject to participate in this study or cannot give informed consent

Design outcomes

Primary

Measure	Time frame
Peak inspiratory presusre checked during mask ventilation with airway	—

Secondary

Measure	Time frame
Tidal volume checked during mask ventilation with airway;Grage of Fiberoptic bronchoscopic findings;Cormack-Lehane grade;Gender;Height;Weight;Body-mass index;ASA classification	—

Countries

Korea, Republic of

Contacts

Public ContactSeongjoo Park

Seoul National University Bundang Hospital

Outcome results