Comparison of the effect of Dexmedetomidine with intravenous Paracetamol on Pain induced by Propofol
Phase 3
Recruiting
- Conditions
- Pain.Pain, not elsewhere classifiedR52.0
- Registration Number
- IRCT20141001019359N14
- Lead Sponsor
- Bojnourd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
The patient must be alert
The patient must be a candidate for surgery under general anesthesia
The patient must not have coagulation problems
The patient must not be allergic to Propofol or the other drugs in the study
The patient must not have cardiovascular problems
Exclusion Criteria
Patients who are addictive or have drug abuse
Patients with hepatic failure
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Propofol injection pain. Timepoint: Measuring pain in a time interval of 5 to 10 seconds during Propofol injection. Method of measurement: Visual Analog Score (VAS) Form of pain and Numeric rating scale (NRS) For rating the pain.
- Secondary Outcome Measures
Name Time Method Mean Arterial Pressure (MAP). Timepoint: Before Propofol injection, 5 seconds after Propofol injection, 30 seconds after Propofol injection. Method of measurement: Use of Monitoring device.;Heart Rate (HR). Timepoint: Before Propofol injection, 5 seconds after Propofol injection, 30 seconds after Propofol injection. Method of measurement: Use of monitoring device.;Length of recovery and return from anesthesia. Timepoint: From extubation until the patient regains consciousness. Method of measurement: Time observation.