Objective Monitoring for Conscious Sedation during Colonoscopy
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0000464
- Lead Sponsor
- Hanyang University Seoul Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Healthy adult
Exclusion Criteria
Excluded from the study were patients with ASA status III or higher, those who refused sedation during colonoscopy, who were hospitalized, and who were pregnant or lactating, as well as patients with an allergy to eggs, beans or latex, with a previous history of alcohol or sedative overdose and adverse events associated with propofol, with sleep apnea or acute gastrointestinal hemorrhage and with a recent history of central nervous system (CNS) abnormalities (e.g. stroke).
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method safety of sedation : blood pressure, pulse rate, saturation, complication of procedure ;efficacy of sedation : satisfaction of patients, doses of sedative drug
- Secondary Outcome Measures
Name Time Method satisfaction of endoscopist