Comparison of the effect of Hyoscine N-Butylbromide on the propofol injection pai
Phase 3
- Conditions
- Pain caused by injection of propofol.
- Registration Number
- IRCT20190109042309N2
- Lead Sponsor
- Sabzevar University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
The patient is a candidate for general anesthetic and surgery
ages 18and 65
Ability to communicate with the research team
Having at least a fifth grade of elementary school
American Society of Anesthesiology Class I, II
patient has the consent and willingness to participate in the research
Exclusion Criteria
Addiction
Sensitive to the drugs studied
Pregnancy
Having Nervous-Muscular Diseases
Having heart disease and history of seizures
Having metabolic and gastrointestinal disorders
Severe nervous and psychiatric disorders
Need for induction of anesthesia and rapid intubation
Kidney disease in the final stage
Liver disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: At the time of induction of anesthesia. Method of measurement: Assessment of Pain Scores of 4-point Verbal Rating Scale (VRS) during Injection of Propofol.
- Secondary Outcome Measures
Name Time Method