Effect of clonidine on intraoperative consumption of propofol
Not Applicable
- Conditions
- general anesthesia.
- Registration Number
- IRCT201202159026N1
- Lead Sponsor
- Anesthesia Research Center, Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
Inclusion criteria
patient informed written consent for entering study; American Society of Anesthesiologists (ASA)
classification score 1 or 2 (I or II); age range of 18 to 65 years and maximum length of surgery
up to 180 minutes
Exclusion criteria
patient disagreement; ASA class>2; SBP>140mmhg or SBP<90mmhg; maximum length of surgery>180min; age<18y or age>65y; cardiac arrhythmias; SaO2<90%; history of egg or propofol sensitivity; multiple trauma; addict in withdrawal phase
coagulopathy.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraoperative consumption of propofol. Timepoint: During operation. Method of measurement: miligram.
- Secondary Outcome Measures
Name Time Method Intraoperative bleeding. Timepoint: During operation. Method of measurement: Mililiter.;Recovery time. Timepoint: At the end of anesthesia. Method of measurement: Minutes.