Comparison of the cold normal saline, lidocaine and metoclopramide and the combination of lidocaine and cold normal saline on pain caused by propofol injectio
Phase 3
- Conditions
- Reduction of pain caused by propofol in anesthesia.
- Registration Number
- IRCT20170404033202N10
- Lead Sponsor
- Sabzevar University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Need for general anesthesia with propofol injection
with consent to participate in evaluation
between 18 and 60 years old
ASA class 1 and 2
Exclusion Criteria
Reluctance to studyPatients
Patients under 20 years and over 60 years
Patients with ASA grade equal to or greater than 3
Patients with advanced heart and lung problems
Sensitivity to any of the drugs used in the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction of pain caused by propofol injection after drug injection. Timepoint: Pain rate at 0, 15 and 30 minutes after propofol injection. Method of measurement: Based on VAS from zero to 10.
- Secondary Outcome Measures
Name Time Method