None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patientes aged 20 to 80 year-old who are scheduled for advanced endoscopic procedure Patients who agree to participate in this trial and voluntarily sign a written consent
Exclusion criteria
Exclusion criteria: 1) Patients sensitized to propofol, midazolam, ethomidate and fat milk 2) Unregulated heart, lung, liver, renal failure 3) Pregnant and lactating women 4) Alcoholics 5) Psychiatric drug users 6) Patients whom other researchers deemed inappropriate for participation in clinical trials
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate patient satisfaction of sedation | — |
Secondary
| Measure | Time frame |
|---|---|
| sedation induced adverse events | — |
Countries
Korea, Republic of
Contacts
Soon Chun Hyang University Hospital Cheonan