comparing the blood level of acute phase protein (Hs-CRP) in two methods of anesthesia
Not Applicable
- Conditions
- anaesthesia.Other complications of anaesthesia
- Registration Number
- IRCT201202067488N2
- Lead Sponsor
- Vice chancellor for research, Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 60
Inclusion Criteria
lower extremity surgery; age 40 to 60 year; male sex.
Exclusion criteria: polymyositis; neurologic disorders; hepatic failure; diabetes (DM); malignancies; pulmonary hypertension; serum Cr above 2 mg/dl; platelet under 150,000; INR under 1.1; steroids consumption within last 6 months; multiple trauma patients.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hs-CRP blood level. Timepoint: before induction of anaesthesia, half an hour after admission to recovery room and next day. Method of measurement: blood anlysis.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: every 10 minutes. Method of measurement: automatic monitoring device.