To evaluate the efficacy of clonidine and tramadol in preventing post spinal anesthesia shivering
Phase 2
- Conditions
- Hypothermy due to anaesthesia.Hypothermy due to anaesthesia
- Registration Number
- IRCT2017031432017N2
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
ASA 1 and 2 patients who underwent spinal anesthesia for elective TUL. Patients who consent to have spinal anesthesia without any local or general infection, heart disease, bradycardia or left ventricular disfunction, kidney, liver disease, seizures, coagulopathy. Patients with BMI <30 with any history of sensitivity or allergy to clonidine and tramadol or history of addiction.
Exclusion criteria: Patients who fail their spinal anesthesia or their spinal anesthesia being off during surgery and underwent general anesthesia or are not satisfied to participate in the study for any reason.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Peripheral temprature. Timepoint: Every 10 minutes up to 120 min later. Method of measurement: Digital thermometer in Centigrade from forehead.;Core temprature. Timepoint: Every 10 minutes up to 120 min later. Method of measurement: Digital thermometer in Centigrade from tympanic membrane erea.;Blood pressure. Timepoint: Every 10 minutes up to 120 min later. Method of measurement: NIBP with digital monitoring in operation room.;Heart rate. Timepoint: Every 10 minutes up to 120 min later. Method of measurement: With digital monitoring in operation room.;Shivering. Timepoint: Every 10 minutes up to 120 min later. Method of measurement: Seeing based on Mahajan category.
- Secondary Outcome Measures
Name Time Method