KCT0000464
Completed
未知
Efficacy of Bispectral Monitoring for Propofol and Midazolam induced Sedation During Colonoscopy
Hanyang University Seoul Hospital0 sites120 target enrollmentTBD
ConditionsNot Applicable
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not Applicable
- Sponsor
- Hanyang University Seoul Hospital
- Enrollment
- 120
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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).
Outcomes
Primary Outcomes
Not specified
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