Influence of time of day on propofol dose for anesthesia inductio
Not Applicable
- Conditions
- All 90 subjects were ASA physical status I or II, between the ages of 18 and 65 years, and were scheduled for elective procedures under general anesthesia
- Registration Number
- JPRN-UMIN000009940
- Lead Sponsor
- Anesthesiology, Fukushima Medical University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Not provided
Exclusion Criteria
1) Allergy to propofol and/or eggs 2) History of neuropsychiatric disorders 3) Taking mind-altering drugs 4) Obese patients whose Body Mass Index are more than 35 kg/m2 5) Hypertension, diabetes, endocrine diseases 6) Deafness
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total propofol induction dose required to achieve loss of consciousness (LOC) Time to LOC
- Secondary Outcome Measures
Name Time Method