JPRN-UMIN000007732
Completed
未知
A randomized parallel-group trial of propofol versus midazolam for sadation during ERCP - A randomized trial of propofol sadation during ERCP
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Hiroshima University hospital
- Enrollment
- 100
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\. Patients who are deemed inappropriate to sedation because of bad general ccondition 2\. Patients with severe cardiovascular or respiratory disorder 3\. Patients who have decompensated liver cirrhosis 4\. Patients who have experienced a serious adverse effect by propofol or midazolam 5\. Patient with known contraindications for propofol or midazolam 6\. Pregnant or potentially pregnant women 7\. Other patients who are in the opinion of the caring investigator unfit for enrollment in the study
Outcomes
Primary Outcomes
Not specified
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