None listed
Conditions
Interventions
Medical Device : Preoxygenation group (Intervention group) : Oxygen was administered at 2 L/min rate using nasal prong 1 minute before intravenous administration of sedatives. If hypoxia (oxygen satur
Sponsors
Uijeongbu Eulji Medical Center, Eulji University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: ? A participant undergoing sedative endoscopy ? A person who understands the purpose and purpose of the study and voluntarily agrees to participate in the study ? A person who has agreed to sedative endoscopy for diagnostic purposes ? Adults aged 40 to 60 and aged 60 to 80 ? A person who has a clear consciousness and can communicate ? Mallampati score of 2 or less
Exclusion criteria
Exclusion criteria: ? American society of anesthesiologists physical classification(ASA) class III or later ? A person with serious cardiovascular disease, respiratory disease, liver disease, kidney disease, cerebrovascular disease, epilepsy, mental illness ? A person with serious gastrointestinal diseases such as gastrointestinal bleeding and gastrointestinal cancer ? A person with baseline oxygen saturation 90% or less ? A person undergoing treatment endoscopy such as ESD and ERCP ? A person who has difficulty communicating ? A person on sleeping pills and sedatives ? A person who had side effects of sleeping pills and sedatives ? A pregnant woman or person likely to be pregnant ? A nursing woman ? Mallampati score 3 or more
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Saturation of partial pressure oxygen, SpO2;Hypoxia (SpO2 90% or less);Anxiety | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure, Pulse rate | — |
Countries
Korea, Republic of
Contacts
Public ContactSu Jung Lee
Uijeongbu Eulji Medical Center, Eulji University
Outcome results
None listed