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randomized prospective clinical trial of sedation in advanced endoscopic procedure

Midazolam plus etomidate sedation versus midazolam plus propofol sedation in advanced endoscopic procedure : a randomized prospective clinical trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002857
Enrollment
210
Registered
2018-05-10
Start date
2016-08-10
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Soon Chun Hyang University Hospital Cheonan
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime frame
Evaluate patient satisfaction of sedation

Secondary

MeasureTime frame
sedation induced adverse events

Countries

Korea, Republic of

Contacts

Public ContactSU JUNG HAN

Soon Chun Hyang University Hospital Cheonan

hsj8380@naver.com+82-41-570-3741

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026