Influence of opioid on the relationship between effect-site concentration of propofol at loss of response and that at maintenance of anesthesia
Not Applicable
- Conditions
- breast tumor and gall stone
- Registration Number
- JPRN-UMIN000042785
- Lead Sponsor
- Kansai Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Not provided
Exclusion Criteria
patients who matched either of following conditions. 1) patients who had severe liver dysfunction or severe renal dysfunction 2) pregnant or lactating women 3) patients who are medicated a drug that had interaction with propofol 4) patients who had neurological disorder 5) patients who showed allergy to propofol 6) ASA-PS III or more 7) obesity (BMI is 35 or more)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method