KCT0001502
Completed
未知
Comparison of predictive performance between modified Marsh propofol model and Schnider propofol model in underweight patients
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Asan Medical Center
- Enrollment
- 30
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. body mass index (BMI) \< 18\.5 (kg/m2\)
- •2\. Hemoglobin \> 9 (mg/dl)
- •3\. Patients undergoing elective surgery under general anesthesia
Exclusion Criteria
- •1\. Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive urine pregnancy test
- •2\. Patients with known hypersensitivity to propofol or to any of the excipients
- •3\. Clinically significant impairment of cardiovascular, respiratory and renal function
- •4\. Patients who are considered by the investigator to be unsuitable to participate in the study for any other reason not mentioned in the inclusion and exclusion criteria.
Outcomes
Primary Outcomes
Not specified
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