Effect of Preoxygenation before Sedative Upper Endoscopy on Oxygen Saturation, Hypoxia, and Anxiety: Age Group Partitioning Randomized Controlled Trials
- Conditions
- Not Applicable
- Registration Number
- KCT0009331
- Lead Sponsor
- ijeongbu Eulji Medical Center, Eulji University
- Brief Summary
Supplementation of preoxygenation before sedative endoscopy had a positive effect on the prevention of hypoxia of the study participants. There was the significant difference of oxygen saturation during sedative procedure between preoxygenation group and control group. In 40-60 years and 60-80 years participants, preoxygenation before sedative upper endoscopy had a positive effect on the prevention of mild desaturation and hypoxia. After the experimental treatment, there was no significant difference in anxiety between preoxygenation group and control group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 116
? 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
? 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
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Saturation of partial pressure oxygen, SpO2;Hypoxia (SpO2 90% or less);Anxiety
- Secondary Outcome Measures
Name Time Method Blood pressure, Pulse rate