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Clinical Trials/KCT0000464
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Observational Study
Sex
All

Investigators

Sponsor
Hanyang University Seoul Hospital

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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