Prospective observational study about factors which influence the blood concentration of propofol during continuous infusio
Not Applicable
- Conditions
- The patients under sedation in ICU by continuous infusion of propofol
- Registration Number
- JPRN-UMIN000015359
- Lead Sponsor
- Department of Clinical Pharmacology, Faculty of Medical Science, Kyushu University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1. Hemoglobin<7 g/dL 2. Patients who is not appropriate to this study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The relationship between the blood concentration of propofol and genetic polymorphism (UGT1A9,CYP2B6), age, sex, blood pressure, liver function, kidney function etc.
- Secondary Outcome Measures
Name Time Method