Effect of intervenous administration of Lidocain and Sufentanyl on reduction of Propofol induced pain during intravenous injectio
Phase 2
- Conditions
- Complications of anaesthesia.other complication of anesthesia
- Registration Number
- IRCT2016040515281N7
- Lead Sponsor
- Vice chancellor for research of International Branch,Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
Patients of 16 to 65 y/o admitted for General Surgery. Exclusion criteria: The patients who received sedative drugs 24 hours before operation; Have drug allergy; Patients with Neurological Disorders or Mental disorders; Drug Addicts; Pregnant women; Who requires a rapid induction of anesthesia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The pain measurment of Intravenous ejction of Propofol If perviously Useage interavenous ejection of Lidocaine. Timepoint: 1 minute after injection of Lidocaine, propofol injected and evalute The pain. Method of measurement: Fill questionare and visual scale.;The measurment of Intravenous ejection of Propofol If perviously Useage of Intravenous Combination of Lidocaine +Sufentanyl. Timepoint: 1 minute after injection of Combination of Lidocaine +Sufentanyl ,Propofol injeceted and evalute The pain. Method of measurement: Fill questionare and visual scale.
- Secondary Outcome Measures
Name Time Method Dermal side effects. Timepoint: From injection time untii ending of recovery time. Method of measurement: Fill questionare.