Pain caused by injection of propofol.
Conditions
Interventions
Intervention 1: Intervention group: Propofol injection after 30 seconds of 20 mg Hyoscine. Intervention 2: Control group: Propofol injection after 60 seconds of 2% lidocaine injection at 40 mg.
Sponsors
Sabzevar University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZohreh Mohamadzadeh Tabrizi
Sabzevar University of Medical Sciences
Outcome results
None listed